geneid | 79841 |
---|---|
ensemblid | ENSG00000165923.17 |
hgncid | 26296 |
symbol | AGBL2 |
name | AGBL carboxypeptidase 2 |
refseq_nuc | NM_024783.4 |
refseq_prot | NP_079059.2 |
ensembl_nuc | ENST00000525123.6 |
ensembl_prot | ENSP00000435582.1 |
mane_status | MANE Select |
chr | chr11 |
start | 47659591 |
end | 47715369 |
strand | - |
ver | v1.2 |
region | chr11:47659591-47715369 |
region5000 | chr11:47654591-47720369 |
regionname0 | AGBL2_chr11_47659591_47715369 |
regionname5000 | AGBL2_chr11_47654591_47720369 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 902 | 207 | 49 | 31 | 98 | 6 | 22 | 82 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002 | 1/0 | 902 | 125 | 25 | 24 | 48 | 8 | 19 | 36 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0003 | 0/0 | 902 | 7 | 1 | 4 | 0 | 1 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0004 | 0/0 | 902 | 3 | 0 | 0 | 2 | 1 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0005 | 0/0 | 902 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0006 | 0/0 | 902 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0007 | 0/0 | 902 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0008 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0009 | 0/0 | 902 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0010 | 0/0 | 902 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0011 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0012 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0013 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2709 | 207 | 49 | 31 | 98 | 6 | 22 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0002 | 1/0 | 2709 | 119 | 22 | 23 | 46 | 8 | 19 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0003 | 0/0 | 2709 | 7 | 1 | 4 | 0 | 1 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0004 | 0/0 | 2709 | 3 | 3 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0005 | 0/0 | 2709 | 3 | 0 | 0 | 2 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0006 | 0/0 | 2709 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0007 | 0/0 | 2709 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0008 | 0/0 | 2709 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0009 | 0/0 | 2709 | 2 | 0 | 1 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0010 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0011 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0012 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0013 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0014 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0015 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0016 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
c0017 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 878 | 229 | 66 | 32 | 100 | 7 | 22 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
t0002 | 0/0 | 878 | 118 | 13 | 28 | 49 | 9 | 19 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
t0003 | 0/0 | 878 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
t0004 | 0/0 | 878 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
t0005 | 0/0 | 878 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
t0006 | 0/0 | 878 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
t0007 | 0/0 | 878 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2709 | 207 | 49 | 31 | 98 | 6 | 22 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0002 | 1/0 | 2709 | 119 | 22 | 23 | 46 | 8 | 19 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0008 | 0/0 | 2709 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0009 | 0/0 | 2709 | 2 | 0 | 1 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0013 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0017 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0003c0003 | 0/0 | 2709 | 7 | 1 | 4 | 0 | 1 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0004c0005 | 0/0 | 2709 | 3 | 0 | 0 | 2 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0005c0006 | 0/0 | 2709 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0006c0004 | 0/0 | 2709 | 3 | 3 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0007c0007 | 0/0 | 2709 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0008c0010 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0009c0016 | 0/0 | 2709 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0010c0014 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0011c0012 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0012c0015 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0013c0011 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3586 | 200 | 46 | 31 | 94 | 6 | 22 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0001c0001t0002 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0001c0001t0003 | 0/0 | 3586 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0001c0001t0005 | 0/0 | 3586 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0001c0001t0006 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0002t0001 | 1/0 | 3586 | 15 | 14 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0002t0002 | 0/0 | 3586 | 103 | 8 | 23 | 46 | 8 | 18 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0002t0007 | 0/0 | 3586 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0008t0004 | 0/0 | 3586 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0009t0002 | 0/0 | 3586 | 2 | 0 | 1 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0013t0002 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0002c0017t0002 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0003c0003t0002 | 0/0 | 3586 | 7 | 1 | 4 | 0 | 1 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0004c0005t0001 | 0/0 | 3586 | 3 | 0 | 0 | 2 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0005c0006t0001 | 0/0 | 3586 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0006c0004t0002 | 0/0 | 3586 | 3 | 3 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0007c0007t0001 | 0/0 | 3586 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0008c0010t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0009c0016t0001 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0010c0014t0001 | 0/0 | 3586 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0011c0012t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0012c0015t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
a0013c0011t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | copy fasta | chr11 | 47654591 | 47720369 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0007g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0008t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0008t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0009t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0009t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0013t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0017t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0004c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0004c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0004c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0005c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0005c0006t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0005c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0006c0004t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0006c0004t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0006c0004t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0007c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0007c0007t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0008c0010t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0009c0016t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0010c0014t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0011c0012t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0012c0015t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0013c0011t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0055 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00099 | hp2 | a0003 | c0003 | t0002 | g0096 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0043 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00544 | hp2 | a0002 | c0009 | t0002 | g0114 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00609 | hp1 | a0004 | c0005 | t0001 | g0305 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0120 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00735 | hp1 | a0003 | c0003 | t0002 | g0121 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0235 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01261 | hp1 | a0003 | c0003 | t0002 | g0354 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0051 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0061 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0045 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01978 | hp2 | a0002 | c0009 | t0002 | g0113 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02148 | hp2 | a0010 | c0014 | t0001 | g0222 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | CDX | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0108 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02258 | hp2 | a0007 | c0007 | t0001 | g0125 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0351 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02451 | hp2 | a0002 | c0017 | t0002 | g0234 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02572 | hp2 | a0013 | c0011 | t0001 | g0210 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0041 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0343 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0328 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02683 | hp2 | a0003 | c0003 | t0002 | g0109 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02723 | hp2 | a0006 | c0004 | t0002 | g0344 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0111 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02896 | hp1 | a0002 | c0008 | t0004 | g0350 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02965 | hp1 | a0008 | c0010 | t0001 | g0002 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0025 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02970 | hp1 | a0007 | c0007 | t0001 | g0124 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0349 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03098 | hp1 | a0002 | c0008 | t0004 | g0352 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03130 | hp2 | a0006 | c0004 | t0002 | g0346 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03486 | hp2 | a0006 | c0004 | t0002 | g0345 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0104 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0052 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04204 | hp1 | a0002 | c0002 | t0007 | g0339 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18747 | hp1 | a0009 | c0016 | t0001 | g0168 | EAS | CHB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | CHB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18941 | hp1 | a0005 | c0006 | t0001 | g0303 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18970 | hp1 | a0005 | c0006 | t0001 | g0304 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18977 | hp1 | a0004 | c0005 | t0001 | g0273 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0355 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19005 | hp1 | a0002 | c0013 | t0002 | g0236 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19007 | hp2 | a0005 | c0006 | t0001 | g0292 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | ASW | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0323 | AFR | ASW | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20752 | hp2 | a0004 | c0005 | t0001 | g0302 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0102 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0013 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | GIH | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01123 | hp1 | a0003 | c0003 | t0002 | g0095 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03471 | hp1 | a0012 | c0015 | t0001 | g0342 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | USA | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG06807 | hp2 | a0011 | c0012 | t0001 | g0324 | AFR | USA | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0283 | REF | REF | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0341 | REF | REF | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47660227
|
T | A | 1 | a0011 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2655A>T | p.Arg885Ser | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 2950/3586 | 2655/2709 | 885/902 | chr11 | 47660227 | ||
chr11:47679976
|
C | A | 9 | a0001a0004a0005others(6): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
missense_variant | MODERATE | c.2013G>T | p.Met671Ile | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/19 | 2308/3586 | 2013/2709 | 671/902 | chr11 | 47679976 | ||
chr11:47690172
|
C | A | 1 | a0010 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.1535G>T | p.Arg512Leu | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1830/3586 | 1535/2709 | 512/902 | chr11 | 47690172 | ||
chr11:47690268
|
A | G | 1 | a0004 | 3 | HG00609.hp1 NA18977.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.1439T>C | p.Leu480Pro | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1734/3586 | 1439/2709 | 480/902 | chr11 | 47690268 | ||
chr11:47690332
|
C | A | 1 | a0012 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1375G>T | p.Ala459Ser | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1670/3586 | 1375/2709 | 459/902 | chr11 | 47690332 | ||
chr11:47690607
|
G | A | 1 | a0009 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1100C>T | p.Thr367Met | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1395/3586 | 1100/2709 | 367/902 | chr11 | 47690607 | ||
chr11:47690661
|
C | T | 1 | a0003 | 7 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(4): Show |
missense_variant | MODERATE | c.1046G>A | p.Arg349His | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1341/3586 | 1046/2709 | 349/902 | chr11 | 47690661 | ||
chr11:47699497
|
G | A | 1 | a0005 | 3 | NA18941.hp1 NA18970.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.643C>T | p.Pro215Ser | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/19 | 938/3586 | 643/2709 | 215/902 | chr11 | 47699497 | ||
chr11:47704575
|
C | T | 1 | a0013 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.554G>A | p.Cys185Tyr | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/19 | 849/3586 | 554/2709 | 185/902 | chr11 | 47704575 | ||
chr11:47704602
|
A | C | 1 | a0006 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.527T>G | p.Leu176Arg | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/19 | 822/3586 | 527/2709 | 176/902 | chr11 | 47704602 | ||
chr11:47705538
|
C | T | 1 | a0008 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128Gln | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/19 | 678/3586 | 383/2709 | 128/902 | chr11 | 47705538 | ||
chr11:47710389
|
C | G | 1 | a0007 | 2 | HG02258.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.220G>C | p.Glu74Gln | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/19 | 515/3586 | 220/2709 | 74/902 | chr11 | 47710389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47660326
|
T | C | 1 | a0002c0008 | 2 | HG02896.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.2556A>G | p.Thr852Thr | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 2851/3586 | 2556/2709 | 852/902 | chr11 | 47660326 | ||
chr11:47690159
|
G | A | 1 | a0002c0013 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1548C>T | p.Ala516Ala | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1843/3586 | 1548/2709 | 516/902 | chr11 | 47690159 | ||
chr11:47699456
|
T | C | 1 | a0002c0009 | 2 | HG00544.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.684A>G | p.Gln228Gln | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/19 | 979/3586 | 684/2709 | 228/902 | chr11 | 47699456 | ||
chr11:47705889
|
G | A | 1 | a0002c0017 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.261C>T | p.His87His | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/19 | 556/3586 | 261/2709 | 87/902 | chr11 | 47705889 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47659661
|
A | T | 1 | a0001c0001t0006 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 512 | chr11 | 47659661 | |||||
chr11:47659708
|
C | T | 1 | a0002c0008t0004 | 2 | HG02896.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*465G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 465 | chr11 | 47659708 | |||||
chr11:47659725
|
T | C | 1 | a0001c0001t0003 | 3 | HG02083.hp2 NA18747.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*448A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 448 | chr11 | 47659725 | |||||
chr11:47659790
|
C | A | 1 | a0001c0001t0005 | 2 | HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 383 | chr11 | 47659790 | |||||
chr11:47659818
|
T | G | 8 | a0001c0001t0002a0002c0002t0002a0002c0002t0007others(5): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 355 | chr11 | 47659818 | |||||
chr11:47714691
|
T | C | 1 | a0002c0002t0007 | 1 | HG04204.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-41A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 2/19 | chr11 | 47714691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47660556
|
A | AT | 221 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.2536-211dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660556 | ||||||
chr11:47660696
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2536-350C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660696 | ||||||
chr11:47660720
|
A | AT | 337 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2536-375dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660720 | ||||||
chr11:47660850
|
C | T | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2536-504G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660850 | ||||||
chr11:47661119
|
T | C | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2536-773A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661119 | ||||||
chr11:47661145
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2536-799T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661145 | ||||||
chr11:47661173
|
A | T | 135 | a0001c0001t0001g0037a0001c0001t0001g0135a0001c0001t0001g0136others(132): Show | 135 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.2536-827T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661173 | ||||||
chr11:47661231
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2536-885G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661231 | ||||||
chr11:47661469
|
G | C | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2536-1123C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661469 | ||||||
chr11:47661509
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2536-1163G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661509 | ||||||
chr11:47661532
|
G | C | 1 | a0001c0001t0001g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2536-1186C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661532 | ||||||
chr11:47661611
|
T | C | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2536-1265A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661611 | ||||||
chr11:47661987
|
T | C | 2 | a0002c0008t0004g0350a0002c0008t0004g0352 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535+1039A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661987 | ||||||
chr11:47662213
|
A | G | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2535+813T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662213 | ||||||
chr11:47662476
|
G | T | 1 | a0002c0002t0002g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2535+550C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662476 | ||||||
chr11:47662495
|
CT | C | 220 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2535+530delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662495 | ||||||
chr11:47662499
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2535+527A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662499 | ||||||
chr11:47662519
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2535+507C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662519 | ||||||
chr11:47662898
|
C | A | 351 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2535+128G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662898 | ||||||
chr11:47662910
|
C | A | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2535+116G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662910 | ||||||
chr11:47663356
|
T | C | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2449-244A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663356 | ||||||
chr11:47663557
|
C | CT | 27 | a0001c0001t0001g0268a0002c0002t0002g0013a0002c0002t0002g0015others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.2449-446dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663557 | ||||||
chr11:47663557
|
CT | C | 9 | a0001c0001t0001g0141a0001c0001t0001g0182a0001c0001t0001g0290others(6): Show | 9 | HG01099.hp2 HG01261.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2449-446delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663557 | ||||||
chr11:47663802
|
C | T | 222 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(219): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.2449-690G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663802 | ||||||
chr11:47663942
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2449-830G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663942 | ||||||
chr11:47664018
|
C | T | 10 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(7): Show | 10 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2449-906G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664018 | ||||||
chr11:47664046
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2449-934C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664046 | ||||||
chr11:47664135
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2449-1023C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664135 | ||||||
chr11:47664175
|
A | C | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2449-1063T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664175 | ||||||
chr11:47664189
|
G | T | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2449-1077C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664189 | ||||||
chr11:47664211
|
TC | T | 7 | a0001c0001t0001g0313a0001c0001t0001g0319a0001c0001t0001g0320others(4): Show | 7 | HG02258.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2449-1100delG | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664211 | ||||||
chr11:47664277
|
C | T | 222 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(219): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.2449-1165G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664277 | ||||||
chr11:47664390
|
G | C | 3 | a0002c0002t0002g0016a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2449-1278C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664390 | ||||||
chr11:47664414
|
G | GT | 11 | a0001c0001t0001g0200a0001c0001t0001g0260a0001c0001t0001g0306others(8): Show | 11 | HG00735.hp1 HG02572.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.2449-1303dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664414 | ||||||
chr11:47664498
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2449-1386C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664498 | ||||||
chr11:47664555
|
C | T | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2449-1443G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664555 | ||||||
chr11:47664605
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2449-1493C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664605 | ||||||
chr11:47664668
|
C | G | 1 | a0002c0002t0002g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2449-1556G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664668 | ||||||
chr11:47664759
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2449-1647A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664759 | ||||||
chr11:47664883
|
T | TA | 6 | a0001c0001t0001g0242a0001c0001t0001g0333a0001c0001t0001g0334others(3): Show | 6 | HG02897.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2449-1772_2449-177 others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664883 | ||||||
chr11:47664884
|
T | A | 16 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0133others(13): Show | 16 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2449-1772A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664884 | ||||||
chr11:47664890
|
T | A | 151 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2449-1778A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664890 | ||||||
chr11:47664890
|
T | TA | 99 | a0001c0001t0001g0037a0001c0001t0001g0198a0001c0001t0001g0199others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2449-1779_2449-177 others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664890 | ||||||
chr11:47664895
|
A | T | 349 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(346): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2449-1783T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664895 | ||||||
chr11:47664896
|
A | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0192a0001c0001t0001g0231others(1): Show | 4 | HG00741.hp1 HG02965.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2449-1784T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664896 | ||||||
chr11:47665067
|
T | C | 1 | a0010c0014t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2448+1889A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665067 | ||||||
chr11:47665247
|
A | G | 1 | a0002c0002t0002g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2448+1709T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665247 | ||||||
chr11:47665595
|
A | G | 85 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2448+1361T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665595 | ||||||
chr11:47665781
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2448+1175T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665781 | ||||||
chr11:47665793
|
T | C | 1 | a0002c0002t0001g0349 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2448+1163A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665793 | ||||||
chr11:47665831
|
G | A | 5 | a0002c0002t0002g0013a0002c0002t0002g0015a0002c0002t0002g0017others(2): Show | 5 | HG00323.hp2 HG01496.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2448+1125C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665831 | ||||||
chr11:47666090
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2448+866T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666090 | ||||||
chr11:47666192
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2448+764C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666192 | ||||||
chr11:47666214
|
C | T | 1 | a0012c0015t0001g0342 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2448+742G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666214 | ||||||
chr11:47666254
|
C | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2448+702G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666254 | ||||||
chr11:47666256
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2448+700A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666256 | ||||||
chr11:47666295
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2448+661C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666295 | ||||||
chr11:47666313
|
G | T | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2448+643C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666313 | ||||||
chr11:47666333
|
G | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448+623C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666333 | ||||||
chr11:47666391
|
C | CA | 114 | a0001c0001t0001g0127a0002c0002t0002g0012a0002c0002t0002g0013others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2448+564dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666391 | ||||||
chr11:47666492
|
C | T | 1 | a0002c0002t0002g0101 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2448+464G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666492 | ||||||
chr11:47666520
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2448+436A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666520 | ||||||
chr11:47666907
|
G | A | 29 | a0001c0001t0001g0237a0001c0001t0001g0242a0001c0001t0001g0310others(26): Show | 29 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.2448+49C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666907 | ||||||
chr11:47667100
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2341-37A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667100 | ||||||
chr11:47667170
|
A | AGCAGAGG others(4): Show |
1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2341-118_2341-108d others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667170 | ||||||
chr11:47667355
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2340+216G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667355 | ||||||
chr11:47667397
|
C | T | 1 | a0002c0002t0007g0339 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2340+174G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667397 | ||||||
chr11:47667399
|
C | T | 1 | a0002c0002t0002g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2340+172G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667399 | ||||||
chr11:47667416
|
C | T | 1 | a0002c0002t0002g0087 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2340+155G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667416 | ||||||
chr11:47667435
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2340+136G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667435 | ||||||
chr11:47667790
|
G | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01071.hp1 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2215-94C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667790 | ||||||
chr11:47667791
|
C | T | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2215-95G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667791 | ||||||
chr11:47667798
|
G | A | 1 | a0002c0002t0002g0092 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2215-102C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667798 | ||||||
chr11:47667880
|
A | G | 1 | a0003c0003t0002g0121 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2215-184T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667880 | ||||||
chr11:47668110
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2215-414C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668110 | ||||||
chr11:47668139
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2215-443C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668139 | ||||||
chr11:47668153
|
A | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG03942.hp1 NA18952.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.2215-457T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668153 | ||||||
chr11:47668166
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2215-470C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668166 | ||||||
chr11:47668208
|
C | CA | 98 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2215-513dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668208 | ||||||
chr11:47668208
|
C | CAA | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0162others(7): Show | 10 | HG00673.hp1 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2215-514_2215-513d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668208 | ||||||
chr11:47668208
|
CA | C | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2215-513delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668208 | ||||||
chr11:47668291
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2214+550C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668291 | ||||||
chr11:47668298
|
G | C | 1 | a0002c0002t0002g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2214+543C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668298 | ||||||
chr11:47669359
|
C | A | 1 | a0001c0001t0001g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2148-452G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669359 | ||||||
chr11:47669487
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2148-580G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669487 | ||||||
chr11:47669551
|
C | T | 1 | a0002c0002t0002g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2148-644G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669551 | ||||||
chr11:47669680
|
TA | T | 133 | a0001c0001t0001g0037a0001c0001t0001g0139a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.2148-774delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669680 | ||||||
chr11:47669701
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2148-794A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669701 | ||||||
chr11:47670006
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2148-1099G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670006 | ||||||
chr11:47670332
|
T | A | 2 | a0002c0002t0002g0022a0002c0002t0002g0024 | 2 | NA18949.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.2148-1425A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670332 | ||||||
chr11:47670333
|
A | T | 4 | a0001c0001t0001g0330a0002c0002t0002g0016a0002c0002t0002g0025others(1): Show | 4 | HG00280.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2148-1426T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670333 | ||||||
chr11:47670427
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2148-1520C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670427 | ||||||
chr11:47670490
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2148-1583T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670490 | ||||||
chr11:47670491
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2148-1584A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670491 | ||||||
chr11:47670526
|
C | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2148-1619G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670526 | ||||||
chr11:47670608
|
C | T | 74 | a0001c0001t0001g0037a0001c0001t0001g0238a0001c0001t0001g0239others(71): Show | 74 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.2148-1701G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670608 | ||||||
chr11:47670694
|
T | TA | 194 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2148-1788dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670694 | ||||||
chr11:47670729
|
C | T | 1 | a0001c0001t0001g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2148-1822G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670729 | ||||||
chr11:47670804
|
G | C | 1 | a0001c0001t0001g0270 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2148-1897C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670804 | ||||||
chr11:47670868
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2148-1961C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670868 | ||||||
chr11:47671206
|
G | T | 1 | a0005c0006t0001g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2148-2299C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671206 | ||||||
chr11:47671332
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2148-2425A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671332 | ||||||
chr11:47671439
|
G | A | 1 | a0002c0002t0002g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2148-2532C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671439 | ||||||
chr11:47671529
|
A | AAAAC | 121 | a0001c0001t0001g0037a0001c0001t0001g0198a0001c0001t0001g0199others(118): Show | 121 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.2148-2626_2148-262 others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671529 | ||||||
chr11:47671630
|
T | G | 1 | a0001c0001t0001g0283 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2148-2723A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671630 | ||||||
chr11:47671724
|
T | TAATTCCC others(7): Show |
1 | a0001c0001t0001g0193 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2148-2831_2148-281 others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671724 | ||||||
chr11:47671950
|
G | C | 1 | a0002c0002t0002g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2148-3043C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671950 | ||||||
chr11:47672101
|
C | T | 3 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024 | 3 | NA18949.hp2 NA19065.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2148-3194G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672101 | ||||||
chr11:47672202
|
C | T | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2148-3295G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672202 | ||||||
chr11:47672292
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2148-3385A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672292 | ||||||
chr11:47672321
|
C | CT | 77 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0015others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2148-3415dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672321 | ||||||
chr11:47672447
|
T | C | 1 | a0002c0002t0002g0059 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2148-3540A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672447 | ||||||
chr11:47672474
|
C | G | 1 | a0002c0002t0001g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2148-3567G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672474 | ||||||
chr11:47672558
|
G | A | 1 | a0003c0003t0002g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2148-3651C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672558 | ||||||
chr11:47672560
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2148-3653G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672560 | ||||||
chr11:47672594
|
C | T | 1 | a0002c0002t0002g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2148-3687G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672594 | ||||||
chr11:47672614
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18968.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2148-3707G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672614 | ||||||
chr11:47672655
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18968.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2148-3748C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672655 | ||||||
chr11:47673022
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2148-4115C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673022 | ||||||
chr11:47673147
|
C | T | 222 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(219): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.2147+4124G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673147 | ||||||
chr11:47673379
|
A | G | 136 | a0001c0001t0001g0037a0001c0001t0001g0135a0001c0001t0001g0136others(133): Show | 136 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.2147+3892T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673379 | ||||||
chr11:47673581
|
T | C | 337 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2147+3690A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673581 | ||||||
chr11:47673793
|
C | CA | 163 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2147+3477dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673793 | ||||||
chr11:47673793
|
C | CAA | 15 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0001g0158others(12): Show | 15 | HG00673.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2147+3476_2147+347 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673793 | ||||||
chr11:47673793
|
CA | C | 117 | a0001c0001t0001g0139a0001c0001t0001g0202a0002c0002t0001g0003others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.2147+3477delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673793 | ||||||
chr11:47673826
|
G | A | 4 | a0002c0002t0002g0074a0002c0002t0002g0076a0002c0002t0002g0077others(1): Show | 4 | HG00438.hp1 NA18964.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2147+3445C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673826 | ||||||
chr11:47673956
|
G | A | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2147+3315C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673956 | ||||||
chr11:47674041
|
G | A | 1 | a0002c0002t0002g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2147+3230C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674041 | ||||||
chr11:47674068
|
G | C | 1 | a0002c0002t0002g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2147+3203C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674068 | ||||||
chr11:47674122
|
A | G | 2 | a0002c0002t0001g0349a0002c0002t0001g0351 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2147+3149T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674122 | ||||||
chr11:47674151
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2147+3120C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674151 | ||||||
chr11:47674155
|
C | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2147+3116G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674155 | ||||||
chr11:47674288
|
G | A | 82 | a0002c0002t0002g0012a0002c0002t0002g0014a0002c0002t0002g0018others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2147+2983C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674288 | ||||||
chr11:47674522
|
G | A | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2147+2749C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674522 | ||||||
chr11:47674566
|
CA | C | 17 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0001g0193others(14): Show | 17 | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2147+2704delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674566 | ||||||
chr11:47674566
|
CAA | C | 91 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.2147+2703_2147+270 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674566 | ||||||
chr11:47674566
|
CAAA | C | 242 | a0001c0001t0001g0037a0001c0001t0001g0139a0001c0001t0001g0141others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2147+2702_2147+270 others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674566 | ||||||
chr11:47674571
|
A | G | 1 | a0002c0002t0002g0050 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2147+2700T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674571 | ||||||
chr11:47674662
|
A | T | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2147+2609T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674662 | ||||||
chr11:47674765
|
C | T | 2 | a0002c0002t0001g0349a0002c0002t0001g0351 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2147+2506G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674765 | ||||||
chr11:47674875
|
C | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0353 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2147+2396G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674875 | ||||||
chr11:47675044
|
A | T | 81 | a0002c0002t0002g0012a0002c0002t0002g0014a0002c0002t0002g0018others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2147+2227T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675044 | ||||||
chr11:47675126
|
TG | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG03942.hp1 NA18952.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.2147+2144delC | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675126 | ||||||
chr11:47675184
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0297 | 2 | NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2147+2087A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675184 | ||||||
chr11:47675194
|
C | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2147+2077G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675194 | ||||||
chr11:47675199
|
C | CT | 8 | a0001c0001t0001g0228a0001c0001t0001g0246a0001c0001t0001g0248others(5): Show | 8 | HG02056.hp1 HG03471.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.2147+2071dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | ||||||
chr11:47675199
|
CT | C | 129 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2147+2071delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | ||||||
chr11:47675199
|
CTT | C | 17 | a0001c0001t0001g0141a0001c0001t0001g0205a0001c0001t0001g0227others(14): Show | 17 | HG01257.hp2 HG01943.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2147+2070_2147+207 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | ||||||
chr11:47675199
|
CTTTT | C | 110 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.2147+2068_2147+207 others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | ||||||
chr11:47675199
|
CTTTTTTT others(6): Show |
C | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2147+2059_2147+207 others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | ||||||
chr11:47675270
|
G | A | 1 | a0002c0002t0002g0105 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2147+2001C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675270 | ||||||
chr11:47675375
|
G | GT | 172 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2147+1895dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675375 | ||||||
chr11:47675375
|
G | GTT | 43 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0136others(40): Show | 43 | HG01071.hp1 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.2147+1894_2147+189 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675375 | ||||||
chr11:47675375
|
GT | G | 95 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0015others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2147+1895delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675375 | ||||||
chr11:47675500
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2147+1771G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675500 | ||||||
chr11:47675695
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01071.hp1 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2147+1576A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675695 | ||||||
chr11:47676041
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2147+1230G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676041 | ||||||
chr11:47676142
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2147+1129C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676142 | ||||||
chr11:47676429
|
A | G | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2147+842T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676429 | ||||||
chr11:47676557
|
C | G | 1 | a0002c0002t0001g0351 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2147+714G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676557 | ||||||
chr11:47676726
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2147+545C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676726 | ||||||
chr11:47676810
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2147+461A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676810 | ||||||
chr11:47676813
|
C | CA | 14 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0178others(11): Show | 14 | HG00735.hp1 HG01175.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2147+457dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676813 | ||||||
chr11:47676813
|
CA | C | 137 | a0001c0001t0001g0037a0001c0001t0001g0139a0001c0001t0001g0149others(134): Show | 137 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.2147+457delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676813 | ||||||
chr11:47676886
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2147+385C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676886 | ||||||
chr11:47677237
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2147+34T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47677237 | ||||||
chr11:47677245
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2147+26T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47677245 | ||||||
chr11:47677450
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2017-49A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677450 | ||||||
chr11:47677475
|
C | T | 1 | a0002c0002t0002g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2017-74G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677475 | ||||||
chr11:47677738
|
C | A | 6 | a0001c0001t0001g0242a0001c0001t0001g0333a0001c0001t0001g0334others(3): Show | 6 | HG02897.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017-337G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677738 | ||||||
chr11:47677846
|
C | A | 30 | a0002c0002t0002g0013a0002c0002t0002g0015a0002c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2017-445G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677846 | ||||||
chr11:47677880
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2017-479G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677880 | ||||||
chr11:47678241
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2017-840G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678241 | ||||||
chr11:47678288
|
C | CTATTT | 22 | a0001c0001t0001g0215a0001c0001t0001g0219a0001c0001t0001g0311others(19): Show | 22 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2017-892_2017-888d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
C | CTATTTTA others(3): Show |
9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017-897_2017-888d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
C | CTATTTTA others(8): Show |
6 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(3): Show | 6 | HG01496.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017-902_2017-888d others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
C | CTATTTTA others(13): Show |
1 | a0001c0001t0001g0237 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2017-907_2017-888d others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
CTATTT | C | 168 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2017-892_2017-888d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
CTATTTTA others(3): Show |
C | 4 | a0001c0001t0001g0293a0006c0004t0002g0344a0006c0004t0002g0345others(1): Show | 4 | HG02723.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-897_2017-888d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
CTATTTTA others(8): Show |
C | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(1): Show | 4 | HG01081.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-902_2017-888d others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678288
|
CTATTTTA others(18): Show |
C | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2017-912_2017-888d others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | ||||||
chr11:47678330
|
A | ATTATTAT others(9): Show |
1 | a0002c0002t0002g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2017-930_2017-929i others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678330 | ||||||
chr11:47678330
|
A | ATTTTTTT others(6): Show |
1 | a0002c0002t0002g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2017-930_2017-929i others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678330 | ||||||
chr11:47678331
|
T | C | 89 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2017-930A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678331 | ||||||
chr11:47678335
|
A | ATT | 32 | a0002c0002t0002g0029a0002c0002t0002g0032a0002c0002t0002g0067others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2017-936_2017-935d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(18): Show |
5 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0002g0061others(2): Show | 5 | HG00099.hp1 HG00544.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(19): Show |
1 | a0002c0002t0002g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(16): Show |
1 | a0002c0002t0002g0087 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(17): Show |
1 | a0002c0002t0002g0068 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(18): Show |
6 | a0002c0002t0002g0028a0002c0002t0002g0030a0002c0002t0002g0060others(3): Show | 6 | HG02074.hp2 HG03669.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(19): Show |
2 | a0002c0002t0002g0014a0002c0002t0002g0036 | 2 | HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2017-935_2017-934i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(16): Show |
2 | a0002c0002t0002g0069a0003c0003t0002g0120 | 2 | HG00639.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2017-935_2017-934i others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(17): Show |
10 | a0002c0002t0002g0012a0002c0002t0002g0059a0002c0002t0002g0065others(7): Show | 10 | HG00735.hp1 HG01261.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(18): Show |
4 | a0002c0002t0002g0070a0002c0002t0002g0077a0002c0002t0002g0090others(1): Show | 4 | HG02257.hp1 NA18990.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(19): Show |
1 | a0003c0003t0002g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2017-935_2017-934i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | ATTTTATT others(20): Show |
1 | a0003c0003t0002g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678335
|
A | T | 2 | a0002c0002t0002g0031a0002c0002t0002g0111 | 2 | HG02735.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2017-934T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | ||||||
chr11:47678338
|
A | ATTATTTT others(11): Show |
2 | a0002c0002t0002g0103a0002c0002t0002g0106 | 2 | NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2017-938_2017-937i others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678338
|
A | ATTATTTT others(16): Show |
1 | a0002c0013t0002g0236 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2017-938_2017-937i others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678338
|
A | ATTTTTTT others(4): Show |
1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2017-938_2017-937i others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678338
|
A | ATTTTTTT others(12): Show |
3 | a0002c0002t0002g0066a0002c0002t0002g0088a0002c0002t0002g0105 | 3 | HG00609.hp2 NA18942.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2017-938_2017-937i others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678338
|
A | ATTTTTTT others(14): Show |
4 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0020others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-938_2017-937i others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678338
|
A | ATTTTTTT others(15): Show |
1 | a0002c0002t0002g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2017-938_2017-937i others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678338
|
A | T | 36 | a0002c0002t0002g0012a0002c0002t0002g0014a0002c0002t0002g0028others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.2017-937T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | ||||||
chr11:47678343
|
A | ATTATTAT others(21): Show |
1 | a0002c0002t0002g0355 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2017-943_2017-942i others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTATTAT others(20): Show |
1 | a0002c0002t0002g0080 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2017-943_2017-942i others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTATTAT others(22): Show |
2 | a0002c0002t0002g0029a0002c0002t0002g0032 | 2 | NA18956.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2017-943_2017-942i others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTATTTT others(19): Show |
3 | a0002c0002t0002g0093a0002c0002t0002g0097a0002c0002t0002g0104 | 3 | HG03491.hp2 HG03492.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2017-943_2017-942i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTATTTT others(20): Show |
12 | a0002c0002t0002g0067a0002c0002t0002g0073a0002c0002t0002g0074others(9): Show | 12 | HG00408.hp1 HG00438.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2017-943_2017-942i others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTATTTT others(21): Show |
11 | a0002c0002t0002g0071a0002c0002t0002g0072a0002c0002t0002g0079others(8): Show | 11 | HG00673.hp2 HG01358.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.2017-943_2017-942i others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTATTTT others(22): Show |
1 | a0002c0002t0002g0084 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2017-943_2017-942i others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | ATTTTATT others(26): Show |
1 | a0002c0002t0002g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2017-943_2017-942i others(35): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678343
|
A | T | 50 | a0002c0002t0002g0012a0002c0002t0002g0014a0002c0002t0002g0018others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.2017-942T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | ||||||
chr11:47678459
|
G | A | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2017-1058C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678459 | ||||||
chr11:47678602
|
G | C | 1 | a0002c0013t0002g0236 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2017-1201C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678602 | ||||||
chr11:47678616
|
G | T | 82 | a0002c0002t0002g0012a0002c0002t0002g0014a0002c0002t0002g0018others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2017-1215C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678616 | ||||||
chr11:47678794
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2016+1179C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678794 | ||||||
chr11:47678812
|
G | C | 351 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2016+1161C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678812 | ||||||
chr11:47678988
|
G | A | 3 | a0002c0002t0002g0016a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2016+985C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678988 | ||||||
chr11:47679037
|
C | T | 1 | a0002c0002t0002g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2016+936G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679037 | ||||||
chr11:47679058
|
C | CA | 20 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0198others(17): Show | 20 | HG01099.hp1 HG01257.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.2016+914dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
C | CAA | 20 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0139others(17): Show | 20 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2016+913_2016+914d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
C | CAAA | 34 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0259others(31): Show | 34 | HG00280.hp2 HG00597.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.2016+912_2016+914d others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
C | CAAAA | 39 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0244others(36): Show | 39 | HG00408.hp2 HG00544.hp1 HG01978.hp1 others(36): Show |
intron_variant | MODIFIER | c.2016+911_2016+914d others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
C | CAAAAA | 7 | a0001c0001t0001g0037a0001c0001t0001g0211a0001c0001t0001g0245others(4): Show | 7 | HG00609.hp1 HG00741.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.2016+910_2016+914d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
C | CAAAAAA | 7 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG02818.hp2 HG03486.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.2016+909_2016+914d others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
CA | C | 73 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.2016+914delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
CAA | C | 125 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.2016+913_2016+914d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679058
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0283 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2016+905_2016+914d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | ||||||
chr11:47679076
|
A | G | 28 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(25): Show | 28 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2016+897T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679076 | ||||||
chr11:47679341
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2016+632A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679341 | ||||||
chr11:47679561
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2016+412T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679561 | ||||||
chr11:47679636
|
A | G | 4 | a0002c0002t0002g0082a0002c0002t0002g0084a0002c0002t0002g0118others(1): Show | 4 | HG02083.hp1 NA18944.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2016+337T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679636 | ||||||
chr11:47680077
|
G | GA | 7 | a0001c0001t0001g0149a0001c0001t0001g0177a0001c0001t0001g0212others(4): Show | 7 | HG02738.hp2 NA18940.hp1 NA18944.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1916-5dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680077 | ||||||
chr11:47680089
|
A | C | 10 | a0002c0002t0002g0027a0002c0002t0002g0033a0002c0002t0002g0034others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1916-16T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680089 | ||||||
chr11:47680267
|
T | C | 115 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1916-194A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680267 | ||||||
chr11:47680378
|
G | A | 1 | a0008c0010t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1916-305C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680378 | ||||||
chr11:47680514
|
C | G | 1 | a0001c0001t0001g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1916-441G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680514 | ||||||
chr11:47680576
|
C | G | 10 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0319others(7): Show | 10 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1916-503G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680576 | ||||||
chr11:47680747
|
C | T | 1 | a0003c0003t0002g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1916-674G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680747 | ||||||
chr11:47680786
|
G | GAAACA | 76 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0198others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.1916-718_1916-714d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | ||||||
chr11:47680786
|
G | GAAACAAA others(3): Show |
148 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1916-723_1916-714d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | ||||||
chr11:47680786
|
G | GAAACAAA others(8): Show |
89 | a0001c0001t0001g0037a0001c0001t0001g0134a0001c0001t0001g0141others(86): Show | 89 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1916-728_1916-714d others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | ||||||
chr11:47680786
|
G | GAAACAAA others(13): Show |
5 | a0001c0001t0001g0243a0001c0001t0001g0259a0001c0001t0001g0261others(2): Show | 5 | HG02083.hp2 HG03831.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-733_1916-714d others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | ||||||
chr11:47680786
|
G | GAAACAAA others(18): Show |
1 | a0001c0001t0001g0275 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1916-738_1916-714d others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | ||||||
chr11:47680786
|
GAAACA | G | 18 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205others(15): Show | 18 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1916-718_1916-714d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | ||||||
chr11:47680795
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1916-722G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680795 | ||||||
chr11:47680843
|
A | G | 104 | a0001c0001t0001g0037a0001c0001t0001g0193a0001c0001t0001g0237others(101): Show | 104 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1916-770T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680843 | ||||||
chr11:47681377
|
CA | C | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1915+591delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47681377 | ||||||
chr11:47681624
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1915+345G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47681624 | ||||||
chr11:47681759
|
G | A | 25 | a0002c0002t0002g0013a0002c0002t0002g0015a0002c0002t0002g0017others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1915+210C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47681759 | ||||||
chr11:47682219
|
A | G | 1 | a0002c0002t0002g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1789-124T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682219 | ||||||
chr11:47682256
|
C | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1789-161G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682256 | ||||||
chr11:47682303
|
GT | G | 25 | a0001c0001t0001g0063a0002c0002t0002g0013a0002c0002t0002g0015others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1789-209delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682303 | ||||||
chr11:47682305
|
T | A | 25 | a0001c0001t0001g0063a0002c0002t0002g0013a0002c0002t0002g0015others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1789-210A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682305 | ||||||
chr11:47682306
|
A | G | 25 | a0001c0001t0001g0063a0002c0002t0002g0013a0002c0002t0002g0015others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1789-211T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682306 | ||||||
chr11:47682391
|
T | C | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1789-296A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682391 | ||||||
chr11:47682648
|
T | G | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1789-553A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682648 | ||||||
chr11:47682859
|
G | A | 1 | a0002c0002t0002g0101 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1789-764C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682859 | ||||||
chr11:47682930
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1789-835A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682930 | ||||||
chr11:47683177
|
C | T | 4 | a0002c0002t0001g0349a0002c0002t0001g0351a0002c0008t0004g0350others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-1082G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683177 | ||||||
chr11:47683191
|
C | T | 3 | a0002c0002t0002g0046a0002c0002t0002g0053a0002c0002t0002g0064 | 3 | HG01175.hp2 HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1789-1096G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683191 | ||||||
chr11:47683463
|
C | A | 221 | a0001c0001t0001g0037a0001c0001t0001g0122a0001c0001t0001g0123others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1789-1368G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683463 | ||||||
chr11:47683851
|
G | A | 9 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1789-1756C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683851 | ||||||
chr11:47683928
|
T | TA | 20 | a0001c0001t0001g0163a0001c0001t0001g0195a0001c0001t0001g0237others(17): Show | 20 | HG00597.hp1 HG01261.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1789-1834dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683928 | ||||||
chr11:47683928
|
TA | T | 80 | a0001c0001t0001g0149a0001c0001t0001g0272a0001c0001t0001g0287others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1789-1834delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683928 | ||||||
chr11:47683978
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1789-1883G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683978 | ||||||
chr11:47684024
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1788+1869C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684024 | ||||||
chr11:47684081
|
TACCCCAT others(9): Show |
T | 1 | a0013c0011t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1788+1796_1788+181 others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684081 | ||||||
chr11:47684511
|
G | A | 1 | a0003c0003t0002g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1788+1382C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684511 | ||||||
chr11:47684534
|
C | T | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+1359G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684534 | ||||||
chr11:47684589
|
A | G | 221 | a0001c0001t0001g0037a0001c0001t0001g0122a0001c0001t0001g0123others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1788+1304T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684589 | ||||||
chr11:47684739
|
A | G | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+1154T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684739 | ||||||
chr11:47684813
|
C | A | 3 | a0002c0002t0002g0016a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1788+1080G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684813 | ||||||
chr11:47685063
|
AG | A | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+829delC | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685063 | ||||||
chr11:47685198
|
C | T | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1788+695G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685198 | ||||||
chr11:47685201
|
C | T | 3 | a0003c0003t0002g0108a0003c0003t0002g0120a0003c0003t0002g0121 | 3 | HG00639.hp2 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1788+692G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685201 | ||||||
chr11:47685385
|
A | G | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1788+508T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685385 | ||||||
chr11:47685432
|
T | C | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1788+461A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685432 | ||||||
chr11:47685525
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1788+368C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685525 | ||||||
chr11:47685604
|
T | C | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+289A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685604 | ||||||
chr11:47685699
|
G | T | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1788+194C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685699 | ||||||
chr11:47685741
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1788+152G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685741 | ||||||
chr11:47686178
|
G | A | 2 | a0002c0002t0002g0016a0002c0002t0002g0025 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1632-129C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686178 | ||||||
chr11:47686294
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1632-245C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686294 | ||||||
chr11:47686376
|
C | T | 1 | a0002c0002t0002g0041 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1632-327G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686376 | ||||||
chr11:47686447
|
G | GT | 72 | a0001c0001t0001g0063a0001c0001t0001g0149a0001c0001t0001g0188others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1632-399dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | ||||||
chr11:47686447
|
G | GTT | 10 | a0002c0002t0002g0029a0002c0002t0002g0031a0002c0002t0002g0032others(7): Show | 10 | HG00642.hp1 HG01081.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1632-400_1632-399d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | ||||||
chr11:47686447
|
G | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138 | 3 | HG02257.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1632-398C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | ||||||
chr11:47686447
|
GT | G | 65 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0127others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1632-399delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | ||||||
chr11:47686580
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1632-531C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686580 | ||||||
chr11:47686674
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1632-625T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686674 | ||||||
chr11:47686678
|
T | C | 337 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1632-629A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686678 | ||||||
chr11:47686688
|
C | T | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1632-639G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686688 | ||||||
chr11:47686731
|
T | C | 337 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1632-682A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686731 | ||||||
chr11:47686959
|
C | CA | 207 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1632-911dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686959 | ||||||
chr11:47686980
|
T | A | 1 | a0002c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1632-931A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686980 | ||||||
chr11:47686999
|
G | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | NA18953.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1632-950C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686999 | ||||||
chr11:47687141
|
AT | A | 110 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1632-1093delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687141 | ||||||
chr11:47687142
|
T | A | 3 | a0002c0002t0002g0099a0002c0002t0002g0102a0002c0002t0002g0112 | 3 | HG01358.hp1 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1632-1093A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687142 | ||||||
chr11:47687363
|
C | T | 347 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1632-1314G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687363 | ||||||
chr11:47687614
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1632-1565C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687614 | ||||||
chr11:47687660
|
C | T | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1632-1611G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687660 | ||||||
chr11:47687807
|
C | CT | 55 | a0001c0001t0001g0063a0001c0001t0001g0294a0002c0002t0002g0013others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1632-1759dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687807 | ||||||
chr11:47687890
|
C | T | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1632-1841G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687890 | ||||||
chr11:47688078
|
G | A | 28 | a0001c0001t0001g0063a0002c0002t0002g0013a0002c0002t0002g0015others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1631+1998C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688078 | ||||||
chr11:47688136
|
A | T | 1 | a0002c0002t0002g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1631+1940T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688136 | ||||||
chr11:47688159
|
G | A | 347 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1631+1917C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688159 | ||||||
chr11:47688173
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1631+1903C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688173 | ||||||
chr11:47688461
|
A | G | 21 | a0002c0002t0002g0014a0002c0002t0002g0022a0002c0002t0002g0023others(18): Show | 21 | HG00099.hp1 HG00544.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1631+1615T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688461 | ||||||
chr11:47688473
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1631+1603A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688473 | ||||||
chr11:47688699
|
T | C | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1631+1377A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688699 | ||||||
chr11:47688762
|
T | G | 3 | a0002c0002t0002g0016a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1631+1314A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688762 | ||||||
chr11:47688783
|
A | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1631+1293T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688783 | ||||||
chr11:47688892
|
T | A | 3 | a0002c0002t0002g0233a0002c0002t0002g0235a0002c0017t0002g0234 | 3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1631+1184A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688892 | ||||||
chr11:47689172
|
G | C | 2 | a0002c0002t0002g0097a0002c0002t0002g0104 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1631+904C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689172 | ||||||
chr11:47689302
|
A | AT | 81 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1631+773dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689302 | ||||||
chr11:47689302
|
AT | A | 103 | a0001c0001t0001g0037a0001c0001t0001g0207a0001c0001t0001g0237others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1631+773delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689302 | ||||||
chr11:47689469
|
T | C | 103 | a0001c0001t0001g0037a0001c0001t0001g0237a0001c0001t0001g0238others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1631+607A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689469 | ||||||
chr11:47689485
|
A | T | 1 | a0001c0001t0001g0179 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1631+591T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689485 | ||||||
chr11:47689957
|
C | T | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1631+119G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689957 | ||||||
chr11:47689992
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1631+84C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689992 | ||||||
chr11:47691084
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.849-226A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691084 | ||||||
chr11:47691097
|
T | C | 3 | a0002c0002t0002g0027a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01255.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.849-239A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691097 | ||||||
chr11:47691099
|
C | CA | 182 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.849-242dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691099 | ||||||
chr11:47691099
|
C | CAA | 144 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0127others(141): Show | 144 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.849-243_849-242dup others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691099 | ||||||
chr11:47691099
|
C | CAAA | 10 | a0001c0001t0001g0238a0001c0001t0001g0330a0002c0002t0002g0050others(7): Show | 10 | HG00280.hp2 HG01192.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-244_849-242dup others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691099 | ||||||
chr11:47691205
|
A | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG00597.hp1 NA18962.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.849-347T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691205 | ||||||
chr11:47691211
|
C | G | 2 | a0002c0002t0002g0097a0002c0002t0002g0104 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.849-353G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691211 | ||||||
chr11:47691447
|
C | A | 28 | a0001c0001t0001g0063a0002c0002t0002g0013a0002c0002t0002g0015others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.849-589G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691447 | ||||||
chr11:47691581
|
G | A | 2 | a0002c0008t0004g0350a0002c0008t0004g0352 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.848+522C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691581 | ||||||
chr11:47691640
|
G | A | 28 | a0001c0001t0001g0063a0002c0002t0002g0013a0002c0002t0002g0015others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.848+463C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691640 | ||||||
chr11:47691710
|
G | GAAAAAAA others(6): Show |
1 | a0004c0005t0001g0305 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.848+380_848+392dup others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691710 | ||||||
chr11:47691725
|
A | AATATATA others(13): Show |
1 | a0008c0010t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.848+377_848+378ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691725 | ||||||
chr11:47691727
|
A | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0008c0010t0001g0002 | 3 | HG02896.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.848+376T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691727 | ||||||
chr11:47691729
|
A | AAAAAAAA others(35): Show |
1 | a0003c0003t0002g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(39): Show |
1 | a0003c0003t0002g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(46): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(36): Show |
1 | a0002c0002t0002g0012 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(43): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(22): Show |
1 | a0002c0002t0002g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(34): Show |
1 | a0003c0003t0002g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(36): Show |
1 | a0002c0002t0002g0112 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(43): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(23): Show |
1 | a0002c0002t0002g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(31): Show |
1 | a0002c0002t0002g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(33): Show |
4 | a0002c0002t0002g0087a0002c0002t0002g0102a0003c0003t0002g0096others(1): Show | 4 | HG00099.hp2 HG00735.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0306 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(22): Show |
3 | a0002c0002t0002g0026a0002c0002t0002g0055a0002c0002t0002g0061 | 3 | HG00099.hp1 HG01517.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
1 | a0002c0002t0002g0106 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0260 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(25): Show |
1 | a0002c0002t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(32): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(27): Show |
1 | a0002c0002t0002g0032 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(34): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(31): Show |
1 | a0002c0002t0002g0084 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(39): Show |
1 | a0002c0002t0002g0090 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(46): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(14): Show |
1 | a0002c0002t0002g0103 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(26): Show |
1 | a0002c0002t0002g0355 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(33): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(34): Show |
1 | a0002c0002t0002g0065 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(36): Show |
1 | a0002c0002t0002g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(43): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
1 | a0005c0006t0001g0304 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(21): Show |
1 | a0002c0002t0002g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(23): Show |
1 | a0002c0002t0002g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(27): Show |
1 | a0002c0002t0002g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(34): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(29): Show |
2 | a0002c0002t0002g0031a0002c0002t0002g0082 | 2 | HG02083.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(31): Show |
2 | a0002c0002t0002g0107a0002c0002t0002g0116 | 2 | HG04199.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(33): Show |
1 | a0002c0002t0002g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0077 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(37): Show |
1 | a0002c0002t0002g0092 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(44): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(39): Show |
1 | a0002c0002t0002g0069 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(46): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(41): Show |
1 | a0002c0002t0002g0036 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(48): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(45): Show |
1 | a0002c0002t0002g0085 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(52): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(12): Show |
1 | a0005c0006t0001g0303 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0262 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(28): Show |
1 | a0002c0002t0002g0080 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(35): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(30): Show |
3 | a0002c0002t0002g0081a0002c0002t0002g0098a0003c0003t0002g0120 | 3 | HG00639.hp2 HG01169.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(37): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(32): Show |
2 | a0002c0002t0002g0060a0002c0002t0002g0067 | 2 | HG00408.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(34): Show |
1 | a0002c0002t0002g0043 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0315a0001c0001t0002g0240 | 2 | HG02886.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
7 | a0001c0001t0001g0275a0001c0001t0001g0277a0001c0001t0001g0326others(4): Show | 7 | HG00323.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0203 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(21): Show |
1 | a0002c0002t0002g0059 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(23): Show |
2 | a0002c0002t0002g0016a0002c0002t0002g0117 | 2 | HG02071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(25): Show |
1 | a0002c0002t0002g0100 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(32): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0063 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(33): Show |
3 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0115 | 3 | HG02523.hp2 NA19009.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0020 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(37): Show |
1 | a0002c0002t0002g0083 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(44): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(12): Show |
5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0238others(2): Show | 5 | HG02300.hp1 NA18953.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0261a0001c0001t0001g0263a0001c0001t0001g0271others(1): Show | 4 | HG00544.hp1 NA18947.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0202 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(16): Show |
6 | a0001c0001t0001g0257a0001c0001t0001g0283a0001c0001t0005g0329others(3): Show | 6 | HG01496.hp2 HG02004.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0330 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(22): Show |
3 | a0002c0002t0002g0030a0002c0002t0002g0053a0002c0009t0002g0113 | 3 | HG01978.hp2 HG02145.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(24): Show |
4 | a0001c0001t0001g0201a0002c0002t0002g0027a0002c0002t0002g0034others(1): Show | 4 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(26): Show |
5 | a0001c0001t0001g0245a0002c0002t0002g0040a0002c0002t0002g0044others(2): Show | 5 | HG01123.hp2 HG01517.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(33): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(28): Show |
2 | a0002c0002t0002g0051a0002c0002t0002g0052 | 2 | HG01515.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(35): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0068 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(34): Show |
1 | a0002c0002t0002g0074 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(9): Show |
8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0187a0001c0001t0001g0266 | 2 | HG03710.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
7 | a0001c0001t0001g0239a0001c0001t0001g0281a0001c0001t0001g0284others(4): Show | 7 | HG02148.hp1 NA18945.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
5 | a0001c0001t0001g0206a0001c0001t0001g0253a0001c0001t0001g0318others(2): Show | 5 | HG00609.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0298a0002c0002t0002g0058a0004c0005t0001g0273 | 3 | HG00408.hp2 HG00642.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0200a0002c0002t0002g0024 | 2 | HG02572.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0199a0002c0002t0002g0022a0002c0002t0002g0062 | 3 | HG02109.hp2 HG03669.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(23): Show |
1 | a0002c0002t0002g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(27): Show |
2 | a0002c0002t0002g0070a0002c0002t0002g0118 | 2 | NA18944.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(34): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(29): Show |
1 | a0002c0002t0002g0078 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(31): Show |
4 | a0002c0002t0002g0071a0002c0002t0002g0089a0002c0002t0002g0119others(1): Show | 4 | HG02451.hp2 NA18993.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(33): Show |
3 | a0002c0002t0002g0019a0002c0002t0002g0023a0002c0002t0002g0066 | 3 | HG03017.hp2 NA18942.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0287 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(37): Show |
1 | a0002c0002t0002g0093 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(44): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(8): Show |
7 | a0001c0001t0001g0149a0001c0001t0001g0154a0001c0001t0001g0167others(4): Show | 7 | HG02293.hp2 HG02897.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0161a0001c0001t0001g0282 | 3 | HG01109.hp1 NA18941.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(12): Show |
2 | a0001c0001t0001g0131a0001c0001t0001g0241 | 2 | HG01192.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0243a0001c0001t0001g0270a0001c0001t0001g0308others(1): Show | 4 | HG02056.hp1 HG03831.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(16): Show |
5 | a0001c0001t0001g0246a0001c0001t0001g0258a0001c0001t0001g0274others(2): Show | 5 | HG01099.hp2 HG01169.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0286 | 2 | HG02273.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0289 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(22): Show |
1 | a0002c0002t0002g0041 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(24): Show |
1 | a0002c0002t0002g0029 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(26): Show |
1 | a0002c0002t0002g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(33): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(32): Show |
2 | a0002c0002t0002g0094a0002c0002t0002g0101 | 2 | HG01258.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0337 | 2 | HG03540.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(9): Show |
5 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0165others(2): Show | 5 | HG02135.hp1 NA18522.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(11): Show |
5 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0156others(2): Show | 5 | HG02135.hp2 HG03453.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
3 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0309 | 3 | HG03704.hp2 NA18991.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
6 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0276others(3): Show | 6 | HG01257.hp2 HG02280.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
4 | a0001c0001t0001g0219a0001c0001t0001g0247a0002c0002t0002g0038others(1): Show | 4 | HG01070.hp1 HG01081.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0204a0002c0002t0002g0064a0002c0009t0002g0114 | 3 | HG00544.hp2 HG01175.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(29): Show |
1 | a0002c0002t0002g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(31): Show |
2 | a0002c0002t0002g0097a0002c0002t0002g0104 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(33): Show |
2 | a0002c0002t0002g0021a0002c0002t0002g0091 | 2 | HG01071.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(6): Show |
2 | a0002c0002t0002g0233a0002c0002t0002g0235 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0140a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG00323.hp1 HG01433.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(10): Show |
5 | a0001c0001t0001g0185a0001c0001t0001g0191a0001c0001t0001g0194others(2): Show | 5 | HG01175.hp1 HG04115.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(12): Show |
5 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0227others(2): Show | 5 | HG02132.hp2 HG02155.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0208a0001c0001t0001g0272 | 2 | HG04199.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(16): Show |
8 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0254others(5): Show | 8 | HG01255.hp1 HG02293.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0198a0001c0001t0001g0252 | 2 | HG02071.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0288 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0237a0002c0002t0007g0339 | 2 | HG02818.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(24): Show |
1 | a0003c0003t0002g0354 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0018 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(9): Show |
9 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0179others(6): Show | 9 | HG02735.hp1 HG02976.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(11): Show |
5 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0001g0230others(2): Show | 5 | HG00597.hp1 HG02572.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0340 | 2 | NA19077.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
4 | a0001c0001t0001g0267a0001c0001t0001g0310a0002c0002t0002g0057others(1): Show | 4 | HG01081.hp1 HG01243.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0331 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(8): Show |
3 | a0001c0001t0001g0141a0001c0001t0001g0338a0007c0007t0001g0125 | 3 | HG01943.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(12): Show |
6 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0155others(3): Show | 6 | HG02630.hp1 HG04204.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0265 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0244a0001c0001t0001g0295a0001c0001t0001g0317 | 3 | HG02145.hp2 NA18957.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0157 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(30): Show |
1 | a0009c0016t0001g0168 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(37): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(7): Show |
4 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0001g0170others(1): Show | 4 | HG00733.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(9): Show |
4 | a0001c0001t0001g0147a0001c0001t0001g0163a0001c0001t0001g0225others(1): Show | 4 | HG02056.hp2 HG02148.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(11): Show |
1 | a0002c0002t0001g0351 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0158a0001c0001t0001g0250 | 2 | HG00673.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
1 | a0006c0004t0002g0346 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0224 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(32): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(10): Show |
2 | a0001c0001t0001g0193a0001c0001t0001g0321 | 2 | HG03471.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(14): Show |
1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0320a0001c0001t0001g0327a0011c0012t0001g0324 | 3 | HG02886.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(22): Show |
1 | a0006c0004t0002g0344 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0212 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0190 | 2 | NA18966.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0322 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0037 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAT others(6): Show |
1 | a0007c0007t0001g0124 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAT others(10): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0312 | 2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAT others(12): Show |
2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0001g0232 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAAAT others(18): Show |
1 | a0002c0008t0004g0352 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAATA others(1): Show |
6 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0218others(3): Show | 6 | HG01109.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAATA others(3): Show |
1 | a0002c0002t0001g0003 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAAATA others(13): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0142 | 2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAATAT others(6): Show |
4 | a0002c0002t0001g0004a0002c0002t0001g0006a0002c0002t0001g0007others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAAATAT others(14): Show |
1 | a0002c0008t0004g0350 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAAATATA others(3): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0188a0002c0002t0001g0009 | 3 | HG01346.hp1 HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | AAATATAT others(14): Show |
1 | a0001c0001t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691729
|
A | T | 4 | a0001c0001t0001g0301a0001c0001t0001g0347a0001c0001t0001g0348others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+374T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | ||||||
chr11:47691731
|
T | A | 3 | a0001c0001t0001g0316a0002c0002t0002g0050a0004c0005t0001g0305 | 3 | HG00609.hp1 HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.848+372A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691731 | ||||||
chr11:47691733
|
T | A | 2 | a0001c0001t0001g0316a0002c0002t0002g0050 | 2 | HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.848+370A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691733 | ||||||
chr11:47691735
|
T | A | 1 | a0002c0002t0002g0050 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.848+368A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691735 | ||||||
chr11:47692002
|
C | T | 1 | a0002c0002t0007g0339 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.848+101G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47692002 | ||||||
chr11:47692404
|
C | CT | 48 | a0001c0001t0001g0063a0001c0001t0001g0126a0001c0001t0001g0127others(45): Show | 48 | HG00438.hp2 HG00642.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.695-149dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | ||||||
chr11:47692404
|
C | CTTT | 52 | a0001c0001t0001g0204a0001c0001t0001g0239a0001c0001t0001g0241others(49): Show | 52 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.695-151_695-149dup others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | ||||||
chr11:47692404
|
C | CTTTT | 52 | a0001c0001t0001g0037a0001c0001t0001g0198a0001c0001t0001g0199others(49): Show | 52 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.695-152_695-149dup others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | ||||||
chr11:47692404
|
CT | C | 80 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0205others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.695-149delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | ||||||
chr11:47692404
|
CTTTTTTT others(5): Show |
C | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.695-160_695-149del others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | ||||||
chr11:47692430
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.695-174C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692430 | ||||||
chr11:47692499
|
C | T | 2 | a0002c0002t0001g0349a0002c0002t0001g0351 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.695-243G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692499 | ||||||
chr11:47692537
|
G | A | 1 | a0003c0003t0002g0121 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.695-281C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692537 | ||||||
chr11:47692603
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0156others(7): Show | 10 | HG02135.hp1 HG03942.hp1 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-347C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692603 | ||||||
chr11:47692659
|
G | A | 1 | a0002c0009t0002g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.695-403C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692659 | ||||||
chr11:47693058
|
G | A | 128 | a0001c0001t0001g0037a0001c0001t0001g0135a0001c0001t0001g0136others(125): Show | 128 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.695-802C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693058 | ||||||
chr11:47693213
|
G | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0353 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.695-957C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693213 | ||||||
chr11:47693538
|
TGA | T | 221 | a0001c0001t0001g0037a0001c0001t0001g0122a0001c0001t0001g0123others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.695-1284_695-1283d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693538 | ||||||
chr11:47693817
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.695-1561C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693817 | ||||||
chr11:47693933
|
T | G | 2 | a0002c0002t0002g0054a0002c0002t0002g0055 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.695-1677A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693933 | ||||||
chr11:47693935
|
A | T | 2 | a0002c0002t0002g0054a0002c0002t0002g0055 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.695-1679T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693935 | ||||||
chr11:47693972
|
T | C | 116 | a0001c0001t0001g0063a0002c0002t0002g0012a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.695-1716A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693972 | ||||||
chr11:47694022
|
T | C | 28 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(25): Show | 28 | HG01071.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.695-1766A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694022 | ||||||
chr11:47694030
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.695-1774A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694030 | ||||||
chr11:47694143
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.695-1887A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694143 | ||||||
chr11:47694229
|
C | CA | 86 | a0001c0001t0001g0131a0001c0001t0001g0147a0001c0001t0001g0198others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.695-1974dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694229 | ||||||
chr11:47694391
|
C | G | 1 | a0002c0002t0001g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.695-2135G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694391 | ||||||
chr11:47694432
|
C | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0188a0001c0001t0001g0231 | 3 | HG00741.hp1 HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.695-2176G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694432 | ||||||
chr11:47694772
|
G | C | 84 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.695-2516C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694772 | ||||||
chr11:47694829
|
T | G | 86 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.695-2573A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694829 | ||||||
chr11:47694875
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0353 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.695-2619C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694875 | ||||||
chr11:47694920
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.695-2664C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694920 | ||||||
chr11:47694969
|
T | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-2713A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694969 | ||||||
chr11:47695048
|
G | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG00597.hp1 NA18962.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.695-2792C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695048 | ||||||
chr11:47695137
|
G | C | 1 | a0002c0002t0002g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.695-2881C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695137 | ||||||
chr11:47695423
|
C | A | 83 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.695-3167G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695423 | ||||||
chr11:47695454
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.695-3198C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695454 | ||||||
chr11:47695475
|
C | CA | 216 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0127others(213): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.695-3220dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695475 | ||||||
chr11:47695475
|
C | CAA | 40 | a0001c0001t0001g0160a0001c0001t0001g0198a0001c0001t0001g0199others(37): Show | 40 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.695-3221_695-3220d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695475 | ||||||
chr11:47695501
|
G | C | 1 | a0008c0010t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.695-3245C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695501 | ||||||
chr11:47695650
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.695-3394A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695650 | ||||||
chr11:47696026
|
A | G | 9 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+3420T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696026 | ||||||
chr11:47696027
|
AAAAAAAA others(3): Show |
A | 9 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+3409_694+3418d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696027 | ||||||
chr11:47696029
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.694+3417T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696029 | ||||||
chr11:47696030
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+3416T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696030 | ||||||
chr11:47696036
|
A | AAAG | 12 | a0001c0001t0001g0128a0001c0001t0001g0187a0001c0001t0001g0201others(9): Show | 12 | HG01071.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.694+3409_694+3410i others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696036 | ||||||
chr11:47696036
|
A | AAG | 58 | a0001c0001t0001g0037a0001c0001t0001g0123a0001c0001t0001g0142others(55): Show | 58 | HG00408.hp1 HG00544.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.694+3409_694+3410i others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696036 | ||||||
chr11:47696036
|
A | G | 7 | a0001c0001t0001g0153a0001c0001t0001g0225a0001c0001t0001g0270others(4): Show | 7 | HG00140.hp2 HG02056.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+3410T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696036 | ||||||
chr11:47696037
|
G | A | 79 | a0001c0001t0001g0037a0001c0001t0001g0123a0001c0001t0001g0128others(76): Show | 79 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.694+3409C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696037 | ||||||
chr11:47696037
|
G | GA | 248 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0129others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.694+3408dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696037 | ||||||
chr11:47696185
|
CA | C | 237 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0127others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.694+3260delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696185 | ||||||
chr11:47696185
|
CAA | C | 105 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(102): Show | 105 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.694+3259_694+3260d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696185 | ||||||
chr11:47696466
|
G | A | 1 | a0002c0002t0002g0070 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.694+2980C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696466 | ||||||
chr11:47696557
|
C | T | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.694+2889G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696557 | ||||||
chr11:47696634
|
A | G | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.694+2812T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696634 | ||||||
chr11:47697150
|
C | A | 337 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.694+2296G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697150 | ||||||
chr11:47697248
|
G | T | 337 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.694+2198C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697248 | ||||||
chr11:47697399
|
C | T | 2 | a0002c0002t0002g0038a0002c0002t0002g0039 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.694+2047G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697399 | ||||||
chr11:47697540
|
CT | C | 121 | a0001c0001t0001g0037a0001c0001t0001g0127a0001c0001t0001g0131others(118): Show | 121 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.694+1905delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697540 | ||||||
chr11:47697540
|
CTT | C | 206 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0123others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.694+1904_694+1905d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697540 | ||||||
chr11:47697631
|
T | C | 351 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.694+1815A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697631 | ||||||
chr11:47697641
|
G | C | 1 | a0002c0008t0004g0352 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.694+1805C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697641 | ||||||
chr11:47697740
|
G | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.694+1706C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697740 | ||||||
chr11:47697835
|
C | A | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.694+1611G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697835 | ||||||
chr11:47697842
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0153 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.694+1604C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697842 | ||||||
chr11:47698042
|
A | G | 8 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+1404T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698042 | ||||||
chr11:47698121
|
C | CA | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.694+1324dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698121 | ||||||
chr11:47698127
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.694+1319C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698127 | ||||||
chr11:47698168
|
A | AT | 119 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0128others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.694+1277dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698168 | ||||||
chr11:47698168
|
A | ATT | 99 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.694+1276_694+1277d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698168 | ||||||
chr11:47698168
|
A | ATTT | 22 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.694+1275_694+1277d others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698168 | ||||||
chr11:47698235
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.694+1211G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698235 | ||||||
chr11:47698676
|
A | G | 117 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.694+770T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698676 | ||||||
chr11:47698889
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.694+557G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698889 | ||||||
chr11:47698925
|
G | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.694+521C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698925 | ||||||
chr11:47698936
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.694+510T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698936 | ||||||
chr11:47698957
|
T | C | 117 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.694+489A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698957 | ||||||
chr11:47698966
|
C | CA | 9 | a0001c0001t0001g0063a0002c0002t0002g0016a0002c0002t0002g0020others(6): Show | 9 | HG00438.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+479dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | ||||||
chr11:47698966
|
CA | C | 15 | a0001c0001t0001g0197a0001c0001t0001g0239a0001c0001t0001g0267others(12): Show | 15 | HG00408.hp2 HG00733.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.694+479delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | ||||||
chr11:47698966
|
CAA | C | 198 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.694+478_694+479del others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | ||||||
chr11:47698966
|
CAAA | C | 9 | a0001c0001t0001g0198a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+477_694+479del others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | ||||||
chr11:47699442
|
A | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | splice_region_variant&intron_variant | LOW | c.694+4T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47699442 | ||||||
chr11:47699667
|
A | C | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-114T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699667 | ||||||
chr11:47699668
|
C | A | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-115G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699668 | ||||||
chr11:47699728
|
A | G | 1 | a0002c0002t0002g0103 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.587-175T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699728 | ||||||
chr11:47699740
|
G | A | 1 | a0002c0002t0002g0083 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.587-187C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699740 | ||||||
chr11:47699760
|
G | A | 102 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.587-207C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699760 | ||||||
chr11:47699975
|
T | G | 4 | a0002c0002t0002g0066a0002c0002t0002g0068a0002c0002t0002g0086others(1): Show | 4 | HG02074.hp2 NA18940.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-422A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699975 | ||||||
chr11:47699992
|
C | CTAT | 117 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-442_587-440dup others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699992 | ||||||
chr11:47700060
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.587-507G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700060 | ||||||
chr11:47700259
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0325 | 2 | HG01261.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.587-706C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700259 | ||||||
chr11:47700293
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.587-740G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700293 | ||||||
chr11:47700334
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.587-781A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700334 | ||||||
chr11:47700357
|
T | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0191 | 2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.587-804A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700357 | ||||||
chr11:47700439
|
T | A | 1 | a0001c0001t0001g0293 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.587-886A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700439 | ||||||
chr11:47700513
|
A | G | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.587-960T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700513 | ||||||
chr11:47700544
|
G | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.587-991C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700544 | ||||||
chr11:47700591
|
AAAAC | A | 199 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.587-1042_587-1039d others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700591 | ||||||
chr11:47700596
|
AAACAAAC others(1): Show |
A | 3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0353 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.587-1051_587-1044d others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700596 | ||||||
chr11:47700600
|
AAACC | A | 16 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(13): Show | 16 | HG02071.hp2 NA18957.hp2 NA18967.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-1051_587-1048d others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700600 | ||||||
chr11:47700608
|
A | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0353 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.587-1055T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700608 | ||||||
chr11:47700839
|
A | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1286T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700839 | ||||||
chr11:47700891
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.587-1338G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700891 | ||||||
chr11:47700939
|
A | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1386T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700939 | ||||||
chr11:47700940
|
T | C | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1387A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700940 | ||||||
chr11:47700941
|
C | T | 1 | a0002c0002t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1388G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700941 | ||||||
chr11:47701019
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-1466C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701019 | ||||||
chr11:47701055
|
C | CA | 16 | a0001c0001t0001g0127a0001c0001t0001g0208a0001c0001t0001g0259others(13): Show | 16 | HG01261.hp2 HG02486.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-1503dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701055 | ||||||
chr11:47701246
|
G | A | 127 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0312others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.587-1693C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701246 | ||||||
chr11:47701267
|
G | A | 117 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-1714C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701267 | ||||||
chr11:47701271
|
C | G | 117 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-1718G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701271 | ||||||
chr11:47701418
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587-1865G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701418 | ||||||
chr11:47701451
|
C | T | 1 | a0002c0002t0002g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.587-1898G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701451 | ||||||
chr11:47701469
|
C | CA | 9 | a0001c0001t0001g0147a0001c0001t0001g0197a0001c0001t0001g0200others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-1917dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701469 | ||||||
chr11:47701469
|
CA | C | 119 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0150others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.587-1917delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701469 | ||||||
chr11:47701469
|
CAA | C | 7 | a0002c0002t0002g0013a0002c0002t0002g0067a0002c0002t0002g0068others(4): Show | 7 | HG00408.hp1 HG01258.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.587-1918_587-1917d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701469 | ||||||
chr11:47701858
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-2305G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701858 | ||||||
chr11:47701886
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.587-2333C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701886 | ||||||
chr11:47701960
|
G | A | 86 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.587-2407C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701960 | ||||||
chr11:47701973
|
CA | C | 338 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.587-2421delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701973 | ||||||
chr11:47701988
|
A | G | 117 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-2435T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701988 | ||||||
chr11:47702261
|
G | A | 3 | a0002c0002t0002g0016a0002c0002t0002g0025a0002c0002t0002g0026 | 3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.586+2282C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702261 | ||||||
chr11:47702386
|
A | G | 220 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.586+2157T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702386 | ||||||
chr11:47702702
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.586+1841G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702702 | ||||||
chr11:47702805
|
C | T | 1 | a0002c0002t0002g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+1738G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702805 | ||||||
chr11:47702843
|
T | C | 1 | a0002c0002t0002g0084 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.586+1700A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702843 | ||||||
chr11:47702929
|
C | T | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.586+1614G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702929 | ||||||
chr11:47703246
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.586+1297C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703246 | ||||||
chr11:47703454
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.586+1089T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703454 | ||||||
chr11:47703754
|
C | T | 84 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.586+789G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703754 | ||||||
chr11:47703925
|
C | CA | 40 | a0001c0001t0001g0037a0001c0001t0001g0193a0001c0001t0001g0197others(37): Show | 40 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.586+617dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703925 | ||||||
chr11:47703940
|
A | AAC | 77 | a0001c0001t0001g0260a0002c0002t0002g0012a0002c0002t0002g0014others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.586+602_586+603ins others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703940 | ||||||
chr11:47703941
|
C | A | 79 | a0001c0001t0001g0260a0002c0002t0002g0012a0002c0002t0002g0014others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.586+602G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703941 | ||||||
chr11:47703942
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.586+601T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703942 | ||||||
chr11:47703962
|
G | A | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+581C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703962 | ||||||
chr11:47703984
|
C | G | 4 | a0002c0002t0002g0054a0002c0002t0002g0055a0002c0002t0002g0056others(1): Show | 4 | HG00099.hp1 HG01433.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+559G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703984 | ||||||
chr11:47704137
|
C | T | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.586+406G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704137 | ||||||
chr11:47704387
|
G | C | 1 | a0002c0002t0002g0061 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.586+156C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704387 | ||||||
chr11:47704439
|
C | T | 2 | a0002c0008t0004g0350a0002c0008t0004g0352 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.586+104G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704439 | ||||||
chr11:47704482
|
C | CA | 17 | a0001c0001t0001g0230a0001c0001t0001g0297a0001c0001t0001g0301others(14): Show | 17 | HG01175.hp2 HG01255.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.586+60dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704482 | ||||||
chr11:47704482
|
CA | C | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(9): Show | 12 | HG01943.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.586+60delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704482 | ||||||
chr11:47704844
|
T | G | 1 | a0002c0002t0002g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.401-116A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47704844 | ||||||
chr11:47705062
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.401-334A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705062 | ||||||
chr11:47705313
|
G | GA | 334 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.400+207dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705313 | ||||||
chr11:47705336
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400+185G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705336 | ||||||
chr11:47705425
|
C | G | 86 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.400+96G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705425 | ||||||
chr11:47705641
|
C | CA | 112 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
splice_region_variant&intron_variant | LOW | c.287-8dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/18 | chr11 | 47705641 | ||||||
chr11:47705641
|
C | CAA | 86 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(83): Show | 86 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(83): Show |
splice_region_variant&intron_variant | LOW | c.287-9_287-8dupTT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/18 | chr11 | 47705641 | ||||||
chr11:47705641
|
C | CAAA | 20 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(17): Show | 20 | HG00408.hp2 HG02071.hp2 HG02523.hp1 others(17): Show |
splice_region_variant&intron_variant | LOW | c.287-10_287-8dupTTT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/18 | chr11 | 47705641 | ||||||
chr11:47705924
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp1 | splice_region_variant&intron_variant | LOW | c.233-7T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47705924 | ||||||
chr11:47706038
|
A | C | 102 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.233-121T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706038 | ||||||
chr11:47706196
|
C | T | 14 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(11): Show | 14 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.233-279G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706196 | ||||||
chr11:47706245
|
G | A | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.233-328C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706245 | ||||||
chr11:47706472
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0230 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.233-555G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706472 | ||||||
chr11:47706497
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.233-580G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706497 | ||||||
chr11:47706522
|
A | T | 101 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(98): Show | 101 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.233-605T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706522 | ||||||
chr11:47706524
|
A | T | 1 | a0002c0009t0002g0113 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.233-607T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706524 | ||||||
chr11:47706824
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233-907C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706824 | ||||||
chr11:47706889
|
TC | T | 113 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(110): Show | 113 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.233-973delG | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706889 | ||||||
chr11:47706890
|
C | CA | 76 | a0001c0001t0001g0141a0002c0002t0001g0005a0002c0002t0001g0009others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(1): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706890
|
C | CAA | 17 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(14): Show | 17 | HG01071.hp2 HG01261.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706890
|
C | CAAA | 7 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706890
|
C | CAT | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706890
|
C | CATA | 8 | a0001c0001t0001g0140a0001c0001t0001g0146a0001c0001t0001g0194others(5): Show | 8 | HG00597.hp1 HG00741.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706890
|
CCA | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0306a0001c0001t0001g0310 | 3 | HG01243.hp1 NA18972.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.233-975_233-974del others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706890
|
CCAAAAAA others(7): Show |
C | 3 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024 | 3 | NA18949.hp2 NA19065.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.233-987_233-974del others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | ||||||
chr11:47706891
|
C | A | 231 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.233-974G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706891 | ||||||
chr11:47706891
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.233-974G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706891 | ||||||
chr11:47707024
|
T | TA | 98 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(95): Show | 98 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.233-1108dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | ||||||
chr11:47707024
|
T | TAA | 8 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-1109_233-1108d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | ||||||
chr11:47707024
|
TA | T | 199 | a0001c0001t0001g0037a0001c0001t0001g0122a0001c0001t0001g0123others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.233-1108delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | ||||||
chr11:47707024
|
TAA | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG01070.hp2 HG01943.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.233-1109_233-1108d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | ||||||
chr11:47707065
|
G | A | 85 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.233-1148C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707065 | ||||||
chr11:47707203
|
C | G | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.233-1286G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707203 | ||||||
chr11:47707372
|
C | T | 104 | a0001c0001t0001g0140a0001c0001t0001g0237a0001c0001t0001g0238others(101): Show | 104 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.233-1455G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707372 | ||||||
chr11:47707432
|
G | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0353 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.233-1515C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707432 | ||||||
chr11:47707572
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233-1655G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707572 | ||||||
chr11:47707599
|
G | A | 1 | a0002c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233-1682C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707599 | ||||||
chr11:47707628
|
G | A | 92 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-1711C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707628 | ||||||
chr11:47707692
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01071.hp1 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.233-1775A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707692 | ||||||
chr11:47707768
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.233-1851G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707768 | ||||||
chr11:47708098
|
C | T | 14 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.233-2181G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708098 | ||||||
chr11:47708218
|
C | T | 114 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.232+2159G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708218 | ||||||
chr11:47708269
|
A | T | 331 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.232+2108T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708269 | ||||||
chr11:47708343
|
C | T | 5 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0020others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+2034G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708343 | ||||||
chr11:47708471
|
CCTTTA | C | 6 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(3): Show | 6 | HG00597.hp2 NA18947.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+1901_232+1905d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708471 | ||||||
chr11:47708514
|
T | G | 3 | a0001c0001t0001g0340a0002c0002t0001g0349a0002c0002t0001g0351 | 3 | HG02451.hp1 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.232+1863A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708514 | ||||||
chr11:47708590
|
C | T | 34 | a0002c0002t0002g0012a0002c0002t0002g0065a0002c0002t0002g0066others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.232+1787G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708590 | ||||||
chr11:47708596
|
G | A | 134 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(131): Show | 134 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.232+1781C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708596 | ||||||
chr11:47708598
|
G | A | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.232+1779C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708598 | ||||||
chr11:47708808
|
G | A | 1 | a0004c0005t0001g0305 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.232+1569C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708808 | ||||||
chr11:47708812
|
C | CA | 16 | a0001c0001t0001g0208a0001c0001t0001g0220a0001c0001t0001g0221others(13): Show | 16 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+1564dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708812 | ||||||
chr11:47708812
|
CA | C | 11 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG00323.hp2 HG02132.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+1564delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708812 | ||||||
chr11:47708857
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+1520G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708857 | ||||||
chr11:47709085
|
G | A | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.232+1292C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709085 | ||||||
chr11:47709213
|
C | T | 16 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(13): Show | 16 | HG02071.hp2 NA18957.hp2 NA18967.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+1164G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709213 | ||||||
chr11:47709399
|
A | C | 1 | a0001c0001t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.232+978T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709399 | ||||||
chr11:47709465
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.232+912T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709465 | ||||||
chr11:47709499
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.232+878A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709499 | ||||||
chr11:47709589
|
C | CT | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+787dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709589 | ||||||
chr11:47709674
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.232+703C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709674 | ||||||
chr11:47709699
|
T | C | 3 | a0002c0002t0002g0233a0002c0002t0002g0235a0002c0017t0002g0234 | 3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.232+678A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709699 | ||||||
chr11:47709778
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.232+599T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709778 | ||||||
chr11:47709836
|
G | C | 28 | a0001c0001t0001g0237a0001c0001t0001g0242a0001c0001t0001g0310others(25): Show | 28 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+541C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709836 | ||||||
chr11:47709871
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.232+506C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709871 | ||||||
chr11:47710155
|
C | T | 1 | a0013c0011t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.232+222G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47710155 | ||||||
chr11:47710183
|
C | T | 1 | a0002c0002t0002g0065 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.232+194G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47710183 | ||||||
chr11:47710299
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.232+78C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47710299 | ||||||
chr11:47710753
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.98-242A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710753 | ||||||
chr11:47710852
|
G | A | 1 | a0002c0002t0001g0349 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.98-341C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710852 | ||||||
chr11:47710909
|
C | CA | 9 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-399dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710909 | ||||||
chr11:47710909
|
CA | C | 323 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.98-399delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710909 | ||||||
chr11:47710909
|
CAA | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0241a0001c0001t0001g0242others(5): Show | 8 | HG02897.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-400_98-399delTT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710909 | ||||||
chr11:47711031
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.98-520T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711031 | ||||||
chr11:47711323
|
G | C | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.98-812C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711323 | ||||||
chr11:47711431
|
C | T | 1 | a0002c0002t0001g0001 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.98-920G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711431 | ||||||
chr11:47711432
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.98-921G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711432 | ||||||
chr11:47711690
|
T | C | 1 | a0013c0011t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.98-1179A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711690 | ||||||
chr11:47711717
|
T | A | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-1206A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711717 | ||||||
chr11:47711814
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.98-1303G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711814 | ||||||
chr11:47711942
|
G | A | 55 | a0002c0002t0002g0012a0002c0002t0002g0065a0002c0002t0002g0066others(52): Show | 55 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.98-1431C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711942 | ||||||
chr11:47712090
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.98-1579T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712090 | ||||||
chr11:47712366
|
C | T | 1 | a0002c0002t0002g0115 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.98-1855G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712366 | ||||||
chr11:47712531
|
G | A | 2 | a0002c0009t0002g0113a0002c0009t0002g0114 | 2 | HG00544.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.97+1753C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712531 | ||||||
chr11:47712606
|
T | C | 2 | a0002c0008t0004g0350a0002c0008t0004g0352 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.97+1678A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712606 | ||||||
chr11:47712792
|
C | G | 2 | a0007c0007t0001g0124a0007c0007t0001g0125 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97+1492G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712792 | ||||||
chr11:47712793
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.97+1491T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712793 | ||||||
chr11:47712825
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.97+1459T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712825 | ||||||
chr11:47712892
|
G | A | 114 | a0001c0001t0001g0037a0001c0001t0001g0063a0002c0002t0002g0012others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.97+1392C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712892 | ||||||
chr11:47712990
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97+1294G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712990 | ||||||
chr11:47713164
|
A | T | 1 | a0002c0002t0002g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.97+1120T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713164 | ||||||
chr11:47713284
|
C | T | 3 | a0006c0004t0002g0344a0006c0004t0002g0345a0006c0004t0002g0346 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.97+1000G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713284 | ||||||
chr11:47713344
|
C | CA | 31 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(28): Show | 31 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.97+939dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713344 | ||||||
chr11:47713581
|
T | A | 351 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.97+703A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713581 | ||||||
chr11:47713602
|
T | A | 217 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.97+682A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713602 | ||||||
chr11:47714074
|
C | T | 1 | a0001c0001t0001g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.97+210G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47714074 | ||||||
chr11:47714452
|
G | A | 1 | a0002c0013t0002g0236 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.34-105C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 2/18 | chr11 | 47714452 | ||||||
chr11:47714471
|
T | C | 102 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.34-124A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 2/18 | chr11 | 47714471 | ||||||
chr11:47714762
|
C | G | 331 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0122others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-100-12G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714762 | ||||||
chr11:47714765
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-100-15C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714765 | ||||||
chr11:47714766
|
A | G | 1 | a0002c0002t0002g0012 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-100-16T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714766 | ||||||
chr11:47714936
|
A | G | 10 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-186T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714936 | ||||||
chr11:47714988
|
G | C | 1 | a0003c0003t0002g0354 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-101+187C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714988 | ||||||
chr11:47715152
|
G | C | 1 | a0002c0002t0002g0355 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-101+23C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47715152 |