geneid | 272 |
---|---|
ensemblid | ENSG00000133805.16 |
hgncid | 470 |
symbol | AMPD3 |
name | adenosine monophosphate deaminase 3 |
refseq_nuc | NM_001025389.2 |
refseq_prot | NP_001020560.1 |
ensembl_nuc | ENST00000396553.7 |
ensembl_prot | ENSP00000379801.2 |
mane_status | MANE Select |
chr | chr11 |
start | 10455264 |
end | 10507579 |
strand | + |
ver | v1.2 |
region | chr11:10455264-10507579 |
region5000 | chr11:10450264-10512579 |
regionname0 | AMPD3_chr11_10455264_10507579 |
regionname5000 | AMPD3_chr11_10450264_10512579 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 767 | 365 | 78 | 69 | 157 | 17 | 42 | 118 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002 | 0/0 | 767 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003 | 0/0 | 767 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004 | 0/0 | 767 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0005 | 0/0 | 767 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0006 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0007 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0008 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0009 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0010 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2304 | 188 | 50 | 39 | 66 | 10 | 22 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0002 | 0/1 | 2304 | 127 | 3 | 23 | 80 | 4 | 16 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0003 | 0/0 | 2304 | 32 | 23 | 5 | 0 | 2 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0004 | 0/0 | 2304 | 6 | 0 | 0 | 6 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0005 | 0/0 | 2304 | 5 | 0 | 0 | 5 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0006 | 0/0 | 2304 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0007 | 0/0 | 2304 | 3 | 0 | 1 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0008 | 0/0 | 2304 | 3 | 0 | 1 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0009 | 0/0 | 2304 | 3 | 0 | 2 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0010 | 0/0 | 2304 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0011 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0012 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0013 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0014 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0015 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0016 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0017 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0018 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0019 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0020 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0021 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0022 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0023 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
c0024 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1886 | 199 | 22 | 41 | 103 | 11 | 21 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0002 | 0/0 | 1886 | 45 | 1 | 11 | 28 | 0 | 5 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0003 | 0/0 | 1886 | 38 | 6 | 0 | 28 | 0 | 4 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0004 | 0/0 | 1888 | 25 | 17 | 6 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0005 | 0/0 | 1886 | 18 | 8 | 4 | 0 | 3 | 3 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0006 | 0/0 | 1886 | 11 | 1 | 5 | 0 | 2 | 3 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0007 | 0/0 | 1886 | 6 | 6 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0008 | 0/0 | 1887 | 6 | 4 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0009 | 0/0 | 1886 | 4 | 0 | 2 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0010 | 0/0 | 1887 | 4 | 4 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0011 | 0/0 | 1888 | 4 | 2 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0012 | 0/0 | 1887 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0013 | 0/0 | 1886 | 3 | 2 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0014 | 1/0 | 1886 | 3 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0015 | 0/0 | 1886 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0016 | 0/0 | 1888 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0017 | 0/0 | 1886 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0018 | 0/0 | 1886 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0019 | 0/0 | 1886 | 2 | 0 | 0 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0020 | 0/0 | 1886 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0021 | 0/0 | 1886 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0022 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0023 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0024 | 0/0 | 1886 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0025 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0026 | 0/0 | 1886 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0027 | 0/0 | 1886 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0028 | 0/0 | 1886 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
t0029 | 0/0 | 1886 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0022 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2304 | 188 | 50 | 39 | 66 | 10 | 22 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002 | 0/1 | 2304 | 127 | 3 | 23 | 80 | 4 | 16 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003 | 0/0 | 2304 | 32 | 23 | 5 | 0 | 2 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0004 | 0/0 | 2304 | 6 | 0 | 0 | 6 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0005 | 0/0 | 2304 | 5 | 0 | 0 | 5 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0007 | 0/0 | 2304 | 3 | 0 | 1 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0010 | 0/0 | 2304 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0013 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0006 | 0/0 | 2304 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0012 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0020 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0024 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003c0008 | 0/0 | 2304 | 3 | 0 | 1 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003c0009 | 0/0 | 2304 | 3 | 0 | 2 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0011 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0014 | 0/0 | 2304 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0015 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0005c0016 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0005c0017 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0006c0019 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0007c0023 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0008c0022 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0009c0021 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0010c0018 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4189 | 92 | 19 | 25 | 28 | 9 | 11 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0002 | 0/0 | 4189 | 32 | 1 | 8 | 19 | 0 | 4 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0003 | 0/0 | 4189 | 23 | 3 | 0 | 18 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0004 | 0/0 | 4191 | 18 | 11 | 5 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0005 | 0/0 | 4189 | 2 | 1 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0007 | 0/0 | 4189 | 4 | 4 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0008 | 0/0 | 4190 | 4 | 3 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0011 | 0/0 | 4191 | 3 | 1 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0013 | 0/0 | 4189 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0014 | 1/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0016 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0020 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0022 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0024 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0025 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0001t0027 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0001 | 0/1 | 4189 | 90 | 1 | 16 | 61 | 1 | 10 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0002 | 0/0 | 4189 | 10 | 0 | 1 | 9 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0003 | 0/0 | 4189 | 12 | 0 | 0 | 10 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0006 | 0/0 | 4189 | 11 | 1 | 5 | 0 | 2 | 3 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0008 | 0/0 | 4190 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0019 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0028 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0002t0029 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0002 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0003 | 0/0 | 4189 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0004 | 0/0 | 4191 | 7 | 6 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0005 | 0/0 | 4189 | 10 | 4 | 2 | 0 | 2 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0007 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0012 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0014 | 0/0 | 4189 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0016 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0017 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0021 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0003t0023 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0004t0001 | 0/0 | 4189 | 6 | 0 | 0 | 6 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0005t0001 | 0/0 | 4189 | 5 | 0 | 0 | 5 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0007t0001 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0007t0002 | 0/0 | 4189 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0010t0005 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0010t0009 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0013t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0001c0013t0011 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0006t0005 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0006t0012 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0012t0008 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0012t0026 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0020t0018 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0002c0024t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003c0008t0009 | 0/0 | 4189 | 2 | 0 | 1 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003c0008t0019 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003c0009t0005 | 0/0 | 4189 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0003c0009t0009 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0011t0015 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0014t0015 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0014t0018 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0004c0015t0007 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0005c0016t0005 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0005c0017t0001 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0006c0019t0013 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0007c0023t0001 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0008c0022t0001 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0009c0021t0001 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
a0010c0018t0001 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | copy fasta | chr11 | 10450264 | 10512579 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0014g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0020g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0022g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0024g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0025g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0027g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0008g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0019g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0028g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0029g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0014g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0017g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0021g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0007t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0007t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0007t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0010t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0010t0009g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0013t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0013t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0006t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0006t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0006t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0012t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0012t0026g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0020t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0024t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0008t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0008t0009g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0008t0019g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0009t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0009t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0009t0009g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0011t0015g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0014t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0014t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0015t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0005c0016t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0005c0017t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0006c0019t0013g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0007c0023t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0008c0022t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0009c0021t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0010c0018t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00099 | hp2 | a0001 | c0003 | t0005 | g0194 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00140 | hp1 | a0001 | c0002 | t0006 | g0065 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00280 | hp2 | a0001 | c0003 | t0005 | g0181 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0087 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00323 | hp2 | a0003 | c0008 | t0009 | g0198 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00639 | hp1 | a0001 | c0003 | t0004 | g0170 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00741 | hp1 | a0001 | c0003 | t0014 | g0007 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01069 | hp1 | a0003 | c0009 | t0005 | g0203 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01071 | hp1 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01071 | hp2 | a0003 | c0009 | t0005 | g0196 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0325 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01106 | hp2 | a0001 | c0007 | t0002 | g0034 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01109 | hp2 | a0001 | c0001 | t0013 | g0030 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01167 | hp1 | a0001 | c0002 | t0006 | g0053 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01168 | hp1 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01169 | hp2 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0350 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0091 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01255 | hp1 | a0001 | c0002 | t0028 | g0098 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01257 | hp2 | a0001 | c0010 | t0009 | g0180 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01361 | hp1 | a0001 | c0002 | t0006 | g0064 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0298 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01496 | hp1 | a0001 | c0003 | t0005 | g0355 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0333 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01516 | hp1 | a0001 | c0002 | t0006 | g0077 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0335 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01884 | hp1 | a0001 | c0003 | t0007 | g0172 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01891 | hp1 | a0005 | c0016 | t0005 | g0199 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0204 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01943 | hp2 | a0001 | c0003 | t0005 | g0128 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02027 | hp1 | a0009 | c0021 | t0001 | g0004 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02055 | hp1 | a0002 | c0020 | t0018 | g0152 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CDX | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CDX | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02257 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02280 | hp1 | a0002 | c0012 | t0026 | g0040 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0346 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02451 | hp2 | a0001 | c0001 | t0022 | g0184 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02572 | hp1 | a0002 | c0012 | t0008 | g0131 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0130 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02602 | hp2 | a0003 | c0009 | t0009 | g0191 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02615 | hp2 | a0005 | c0017 | t0001 | g0341 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0185 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02630 | hp2 | a0004 | c0014 | t0015 | g0168 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0205 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0323 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02717 | hp1 | a0006 | c0019 | t0013 | g0336 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02717 | hp2 | a0004 | c0014 | t0018 | g0169 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02723 | hp1 | a0001 | c0003 | t0021 | g0200 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0147 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02735 | hp2 | a0001 | c0010 | t0005 | g0202 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02738 | hp2 | a0001 | c0007 | t0002 | g0126 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02809 | hp1 | a0002 | c0024 | t0010 | g0042 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0003 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02818 | hp2 | a0002 | c0006 | t0005 | g0206 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0003 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02895 | hp1 | a0004 | c0011 | t0015 | g0017 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02896 | hp1 | a0002 | c0006 | t0005 | g0207 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02897 | hp2 | a0004 | c0011 | t0015 | g0017 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0353 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02965 | hp1 | a0001 | c0003 | t0005 | g0129 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02976 | hp1 | a0001 | c0003 | t0017 | g0188 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0156 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03041 | hp1 | a0001 | c0001 | t0025 | g0317 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0177 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03139 | hp1 | a0001 | c0013 | t0010 | g0175 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0348 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03195 | hp1 | a0001 | c0003 | t0010 | g0171 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03195 | hp2 | a0001 | c0013 | t0011 | g0178 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0352 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03225 | hp2 | a0001 | c0003 | t0014 | g0007 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03486 | hp2 | a0001 | c0003 | t0012 | g0187 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03540 | hp1 | a0004 | c0015 | t0007 | g0174 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03540 | hp2 | a0010 | c0018 | t0001 | g0340 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03579 | hp2 | a0001 | c0003 | t0017 | g0186 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0343 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03669 | hp1 | a0001 | c0001 | t0008 | g0138 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03688 | hp1 | a0001 | c0002 | t0008 | g0022 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0304 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0155 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03831 | hp2 | a0003 | c0008 | t0019 | g0167 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0286 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03942 | hp2 | a0001 | c0002 | t0006 | g0052 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0327 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0329 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04184 | hp1 | a0001 | c0002 | t0006 | g0075 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04184 | hp2 | a0001 | c0003 | t0005 | g0195 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04199 | hp1 | a0001 | c0001 | t0011 | g0162 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04199 | hp2 | a0001 | c0003 | t0005 | g0192 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04204 | hp2 | a0001 | c0002 | t0006 | g0324 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0190 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18522 | hp2 | a0001 | c0002 | t0029 | g0118 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18906 | hp2 | a0001 | c0003 | t0012 | g0189 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18969 | hp2 | a0001 | c0004 | t0001 | g0288 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18974 | hp2 | a0001 | c0005 | t0001 | g0221 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18985 | hp1 | a0001 | c0005 | t0001 | g0253 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18991 | hp1 | a0001 | c0005 | t0001 | g0215 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18991 | hp2 | a0008 | c0022 | t0001 | g0247 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18994 | hp1 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18994 | hp2 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0308 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19007 | hp1 | a0007 | c0023 | t0001 | g0228 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19011 | hp2 | a0001 | c0001 | t0027 | g0231 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19030 | hp1 | a0002 | c0006 | t0012 | g0208 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19055 | hp1 | a0001 | c0005 | t0001 | g0212 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19064 | hp2 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19079 | hp2 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0223 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19085 | hp2 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19240 | hp2 | a0001 | c0003 | t0016 | g0201 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20129 | hp1 | a0001 | c0003 | t0005 | g0193 | AFR | ASW | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ASW | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20752 | hp2 | a0001 | c0002 | t0019 | g0148 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0183 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20805 | hp2 | a0001 | c0007 | t0001 | g0334 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | GIH | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01123 | hp1 | a0003 | c0008 | t0009 | g0197 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0038 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02559 | hp2 | a0001 | c0002 | t0006 | g0306 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03471 | hp1 | a0001 | c0003 | t0023 | g0003 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG06807 | hp2 | a0001 | c0003 | t0005 | g0182 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20300 | hp1 | a0001 | c0003 | t0004 | g0173 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0137 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA21309 | hp2 | a0001 | c0001 | t0024 | g0302 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0299 | REF | REF | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0014 | g0135 | REF | REF | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10482189
|
C | T | 1 | a0003 | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
missense_variant | MODERATE | c.553C>T | p.Arg185Trp | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/15 | 743/4189 | 553/2304 | 185/767 | chr11 | 10482189 | ||
chr11:10493476
|
G | A | 1 | a0005 | 2 | HG01891.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1067G>A | p.Arg356Gln | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1257/4189 | 1067/2304 | 356/767 | chr11 | 10493476 | ||
chr11:10493490
|
G | A | 2 | a0004a0010 | 6 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
missense_variant | MODERATE | c.1081G>A | p.Gly361Ser | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1271/4189 | 1081/2304 | 361/767 | chr11 | 10493490 | ||
chr11:10495666
|
T | C | 3 | a0002a0004a0006 | 13 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
missense_variant | MODERATE | c.1363T>C | p.Tyr455His | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/15 | 1553/4189 | 1363/2304 | 455/767 | chr11 | 10495666 | ||
chr11:10501519
|
G | A | 2 | a0006a0009 | 2 | HG02027.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.1771G>A | p.Gly591Ser | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/15 | 1961/4189 | 1771/2304 | 591/767 | chr11 | 10501519 | ||
chr11:10504654
|
C | T | 1 | a0008 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.2122C>T | p.His708Tyr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/15 | 2312/4189 | 2122/2304 | 708/767 | chr11 | 10504654 | ||
chr11:10505865
|
T | C | 1 | a0007 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.2285T>C | p.Ile762Thr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 2475/4189 | 2285/2304 | 762/767 | chr11 | 10505865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10478727
|
C | T | 1 | a0001c0005 | 5 | NA18974.hp2 NA18985.hp1 NA18991.hp1 others(2): Show |
synonymous_variant | LOW | c.423C>T | p.Ala141Ala | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/15 | 613/4189 | 423/2304 | 141/767 | chr11 | 10478727 | ||
chr11:10482209
|
G | A | 8 | a0001c0003a0001c0010a0001c0013others(5): Show | 45 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
synonymous_variant | LOW | c.573G>A | p.Pro191Pro | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/15 | 763/4189 | 573/2304 | 191/767 | chr11 | 10482209 | ||
chr11:10484899
|
C | T | 5 | a0001c0013a0002c0012a0002c0024others(2): Show | 8 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.669C>T | p.His223His | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/15 | 859/4189 | 669/2304 | 223/767 | chr11 | 10484899 | ||
chr11:10493369
|
G | A | 1 | a0001c0004 | 6 | NA18969.hp2 NA18994.hp2 NA19000.hp2 others(3): Show |
synonymous_variant | LOW | c.960G>A | p.Ala320Ala | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1150/4189 | 960/2304 | 320/767 | chr11 | 10493369 | ||
chr11:10493540
|
C | T | 3 | a0004c0011a0004c0014a0004c0015 | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.1131C>T | p.His377His | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1321/4189 | 1131/2304 | 377/767 | chr11 | 10493540 | ||
chr11:10500202
|
C | T | 1 | a0001c0007 | 3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.1674C>T | p.Tyr558Tyr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/15 | 1864/4189 | 1674/2304 | 558/767 | chr11 | 10500202 | ||
chr11:10500217
|
T | C | 7 | a0001c0002a0001c0004a0001c0005others(4): Show | 145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
synonymous_variant | LOW | c.1689T>C | p.Tyr563Tyr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/15 | 1879/4189 | 1689/2304 | 563/767 | chr11 | 10500217 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10455351
|
T | C | 44 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(41): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
5_prime_UTR_variant | MODIFIER | c.-103T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/15 | 6169 | chr11 | 10455351 | |||||
chr11:10455366
|
G | T | 6 | a0001c0001t0002a0001c0002t0002a0001c0002t0028others(3): Show | 47 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/15 | 6154 | chr11 | 10455366 | |||||
chr11:10455372
|
T | G | 17 | a0001c0001t0005a0001c0001t0016a0001c0001t0020others(14): Show | 32 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-82T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/15 | 6148 | chr11 | 10455372 | |||||
chr11:10506221
|
G | C | 1 | a0001c0003t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 337 | chr11 | 10506221 | |||||
chr11:10506323
|
G | C | 1 | a0001c0001t0020 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*439G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 439 | chr11 | 10506323 | |||||
chr11:10506411
|
C | T | 1 | a0001c0002t0029 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 527 | chr11 | 10506411 | |||||
chr11:10506578
|
A | G | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
3_prime_UTR_variant | MODIFIER | c.*694A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 694 | chr11 | 10506578 | |||||
chr11:10506895
|
T | TTG | 9 | a0001c0001t0004a0001c0001t0011a0001c0001t0016others(6): Show | 34 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1032dupGT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1033 | INFO_REALIGN_3_PRIME | chr11 | 10506895 | ||||
chr11:10506936
|
A | G | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1052 | chr11 | 10506936 | |||||
chr11:10506954
|
A | G | 7 | a0001c0002t0006a0001c0002t0019a0001c0002t0028others(4): Show | 18 | HG00140.hp1 HG00323.hp2 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1070A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1070 | chr11 | 10506954 | |||||
chr11:10506974
|
A | G | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*1090A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1090 | chr11 | 10506974 | |||||
chr11:10507105
|
T | C | 1 | a0002c0012t0026 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1221 | chr11 | 10507105 | |||||
chr11:10507129
|
G | A | 1 | a0001c0001t0025 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1245G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1245 | chr11 | 10507129 | |||||
chr11:10507285
|
T | TA | 9 | a0001c0001t0008a0001c0001t0010a0001c0002t0008others(6): Show | 13 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1402dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1403 | INFO_REALIGN_3_PRIME | chr11 | 10507285 | ||||
chr11:10507442
|
C | G | 1 | a0001c0001t0027 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1558C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1558 | chr11 | 10507442 | |||||
chr11:10507469
|
G | A | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*1585G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1585 | chr11 | 10507469 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10455493
|
G | C | 1 | a0001c0001t0013g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6+45G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455493 | ||||||
chr11:10455580
|
C | T | 186 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0209others(183): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-6+132C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455580 | ||||||
chr11:10455829
|
G | T | 1 | a0001c0003t0005g0355 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-6+381G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455829 | ||||||
chr11:10455853
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-6+405G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455853 | ||||||
chr11:10456177
|
A | G | 1 | a0001c0002t0002g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-6+729A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456177 | ||||||
chr11:10456304
|
C | G | 1 | a0001c0002t0001g0354 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-6+856C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456304 | ||||||
chr11:10456392
|
G | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6+944G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456392 | ||||||
chr11:10456681
|
C | T | 167 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(164): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-6+1233C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456681 | ||||||
chr11:10456722
|
G | C | 3 | a0001c0003t0005g0181a0001c0003t0005g0182a0001c0010t0009g0180 | 3 | HG00280.hp2 HG01257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-6+1274G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456722 | ||||||
chr11:10456961
|
T | A | 277 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(274): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.-6+1513T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456961 | ||||||
chr11:10456977
|
C | CT | 64 | a0001c0001t0001g0024a0001c0001t0001g0124a0001c0001t0001g0125others(61): Show | 69 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.-6+1547dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10456977 | |||||
chr11:10456977
|
C | CTT | 10 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0001g0351others(7): Show | 10 | HG01192.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6+1546_-6+1547dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10456977 | |||||
chr11:10456977
|
CT | C | 8 | a0001c0001t0003g0127a0001c0001t0004g0035a0001c0002t0002g0033others(5): Show | 9 | HG00741.hp1 HG01106.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+1547delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10456977 | |||||
chr11:10457032
|
C | T | 3 | a0001c0001t0008g0166a0004c0014t0015g0168a0004c0014t0018g0169 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-6+1584C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457032 | ||||||
chr11:10457045
|
A | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6+1597A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457045 | ||||||
chr11:10457241
|
T | C | 32 | a0001c0001t0005g0190a0001c0001t0016g0130a0001c0001t0020g0204others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.-6+1793T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457241 | ||||||
chr11:10457698
|
C | A | 65 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(62): Show | 74 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-6+2250C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457698 | ||||||
chr11:10457701
|
C | T | 1 | a0001c0002t0001g0307 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-6+2253C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457701 | ||||||
chr11:10457723
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-6+2275C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457723 | ||||||
chr11:10457756
|
A | G | 68 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(65): Show | 77 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-6+2308A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457756 | ||||||
chr11:10457788
|
G | A | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-6+2340G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457788 | ||||||
chr11:10457827
|
C | T | 67 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(64): Show | 76 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.-6+2379C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457827 | ||||||
chr11:10457856
|
C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+2408C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457856 | ||||||
chr11:10457938
|
GATCTGGC others(3): Show |
G | 68 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(65): Show | 77 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-6+2492_-6+2501del others(10): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10457938 | |||||
chr11:10457941
|
C | G | 1 | a0001c0002t0001g0346 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-6+2493C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457941 | ||||||
chr11:10458002
|
G | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0007g0348 | 3 | HG02451.hp1 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-6+2554G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458002 | ||||||
chr11:10458030
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(40): Show | 48 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-6+2582C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458030 | ||||||
chr11:10458175
|
A | T | 3 | a0002c0006t0005g0206a0002c0006t0005g0207a0002c0006t0012g0208 | 3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-6+2727A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458175 | ||||||
chr11:10458254
|
T | TA | 66 | a0001c0001t0001g0036a0001c0001t0001g0331a0001c0001t0001g0332others(63): Show | 72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6+2829dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | |||||
chr11:10458254
|
T | TAA | 37 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0293others(34): Show | 41 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.-6+2828_-6+2829dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | |||||
chr11:10458254
|
T | TAAA | 111 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0222others(108): Show | 120 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-6+2827_-6+2829dup others(3): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | |||||
chr11:10458254
|
T | TAAAA | 35 | a0001c0001t0001g0214a0001c0001t0005g0190a0001c0001t0016g0130others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+2826_-6+2829dup others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | |||||
chr11:10458296
|
GCTCC | G | 356 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(353): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-6+2863_-6+2866del others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458296 | |||||
chr11:10458305
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0004g0024 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-6+2857C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458305 | ||||||
chr11:10458308
|
C | T | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 5 | HG00140.hp2 HG00738.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2860C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458308 | ||||||
chr11:10458353
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6+2905C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458353 | ||||||
chr11:10458502
|
C | T | 2 | a0001c0003t0003g0032a0001c0003t0014g0007 | 3 | HG00741.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-5-3013C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458502 | ||||||
chr11:10458777
|
G | A | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-2738G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458777 | ||||||
chr11:10458880
|
A | G | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5-2635A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458880 | ||||||
chr11:10458919
|
C | T | 31 | a0001c0001t0005g0190a0001c0001t0016g0130a0001c0001t0022g0184others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-5-2596C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458919 | ||||||
chr11:10458936
|
T | G | 2 | a0001c0003t0003g0032a0001c0003t0014g0007 | 3 | HG00741.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-5-2579T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458936 | ||||||
chr11:10458945
|
G | T | 1 | a0001c0002t0001g0291 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-5-2570G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458945 | ||||||
chr11:10459216
|
G | A | 31 | a0001c0001t0005g0190a0001c0001t0016g0130a0001c0001t0020g0204others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-5-2299G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459216 | ||||||
chr11:10459462
|
T | G | 1 | a0001c0003t0021g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-5-2053T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459462 | ||||||
chr11:10459471
|
G | A | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5-2044G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459471 | ||||||
chr11:10459592
|
A | G | 66 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(63): Show | 74 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-5-1923A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459592 | ||||||
chr11:10459632
|
A | C | 1 | a0001c0002t0001g0290 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-5-1883A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459632 | ||||||
chr11:10459669
|
A | G | 109 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(106): Show | 122 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-5-1846A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459669 | ||||||
chr11:10459727
|
G | C | 14 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 15 | HG00639.hp2 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5-1788G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459727 | ||||||
chr11:10459749
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(40): Show | 48 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5-1766C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459749 | ||||||
chr11:10459796
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-5-1719G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459796 | ||||||
chr11:10459995
|
T | G | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-1520T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459995 | ||||||
chr11:10460040
|
A | AAATATAT others(18): Show |
1 | a0001c0002t0001g0289 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-5-1474_-5-1450dup others(25): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460040 | |||||
chr11:10460040
|
AAATATAT others(9): Show |
A | 33 | a0001c0001t0005g0190a0001c0001t0016g0130a0001c0001t0020g0204others(30): Show | 34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-1448_-5-1433del others(16): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460040 | |||||
chr11:10460054
|
T | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0293others(21): Show | 27 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-5-1461T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460054 | ||||||
chr11:10460066
|
T | A | 157 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(154): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-5-1449T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460066 | ||||||
chr11:10460083
|
T | TTA | 10 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0014others(7): Show | 11 | HG00558.hp1 HG02080.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-1416_-5-1415dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460083 | |||||
chr11:10460083
|
TTA | T | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-1416_-5-1415del others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460083 | |||||
chr11:10460091
|
A | G | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-1424A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460091 | ||||||
chr11:10460099
|
A | T | 1 | a0001c0001t0001g0345 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-5-1416A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460099 | ||||||
chr11:10460101
|
T | A | 3 | a0001c0001t0008g0166a0004c0014t0015g0168a0004c0014t0018g0169 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-5-1414T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460101 | ||||||
chr11:10460120
|
C | T | 156 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(153): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-5-1395C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460120 | ||||||
chr11:10460155
|
T | A | 4 | a0001c0001t0002g0014a0001c0001t0002g0088a0001c0001t0002g0092others(1): Show | 5 | HG00558.hp1 HG02132.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-1360T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460155 | ||||||
chr11:10460260
|
G | A | 1 | a0001c0002t0028g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-5-1255G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460260 | ||||||
chr11:10460395
|
G | A | 12 | a0001c0001t0001g0176a0001c0003t0004g0003a0001c0003t0004g0023others(9): Show | 14 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5-1120G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460395 | ||||||
chr11:10460409
|
CT | C | 202 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(199): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-5-1091delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460409 | |||||
chr11:10460456
|
G | T | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-5-1059G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460456 | ||||||
chr11:10460635
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-880C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460635 | ||||||
chr11:10460639
|
C | T | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5-876C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460639 | ||||||
chr11:10460648
|
A | G | 55 | a0001c0001t0001g0176a0001c0001t0001g0209a0001c0001t0001g0210others(52): Show | 61 | HG00423.hp2 HG00639.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.-5-867A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460648 | ||||||
chr11:10460700
|
C | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-815C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460700 | ||||||
chr11:10460789
|
A | G | 1 | a0001c0001t0011g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-5-726A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460789 | ||||||
chr11:10460878
|
T | G | 33 | a0001c0001t0005g0190a0001c0001t0016g0130a0001c0001t0020g0204others(30): Show | 34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-637T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460878 | ||||||
chr11:10460981
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-5-534A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460981 | ||||||
chr11:10461129
|
A | G | 1 | a0001c0002t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5-386A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461129 | ||||||
chr11:10461187
|
C | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5-328C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461187 | ||||||
chr11:10461254
|
A | G | 1 | a0001c0002t0029g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-5-261A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461254 | ||||||
chr11:10461374
|
C | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-141C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461374 | ||||||
chr11:10461428
|
G | C | 2 | a0001c0001t0001g0222a0001c0005t0001g0223 | 2 | NA18997.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-5-87G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461428 | ||||||
chr11:10461429
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0123 | 2 | HG00733.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-5-86G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461429 | ||||||
chr11:10461447
|
T | C | 1 | a0001c0002t0001g0224 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-5-68T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461447 | ||||||
chr11:10461765
|
G | A | 2 | a0001c0001t0001g0225a0001c0002t0001g0226 | 2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.221+25G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10461765 | ||||||
chr11:10461912
|
G | A | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.221+172G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10461912 | ||||||
chr11:10461993
|
C | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.221+253C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10461993 | ||||||
chr11:10462080
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.221+340T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462080 | ||||||
chr11:10462203
|
C | T | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+463C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462203 | ||||||
chr11:10462241
|
A | G | 45 | a0001c0001t0001g0083a0001c0001t0003g0018a0001c0001t0003g0019others(42): Show | 51 | HG00423.hp2 HG00609.hp2 HG02040.hp1 others(48): Show |
intron_variant | MODIFIER | c.221+501A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462241 | ||||||
chr11:10462338
|
G | A | 1 | a0001c0002t0001g0227 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.221+598G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462338 | ||||||
chr11:10462524
|
T | G | 45 | a0001c0001t0001g0083a0001c0001t0003g0018a0001c0001t0003g0019others(42): Show | 51 | HG00423.hp2 HG00609.hp2 HG02040.hp1 others(48): Show |
intron_variant | MODIFIER | c.221+784T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462524 | ||||||
chr11:10462706
|
G | A | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+966G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462706 | ||||||
chr11:10462725
|
G | GAGAGAAA others(19): Show |
1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221+987_221+1012du others(27): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10462725 | |||||
chr11:10462817
|
C | A | 4 | a0001c0002t0001g0229a0001c0002t0001g0289a0001c0002t0001g0307others(1): Show | 4 | HG02155.hp1 NA18941.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1077C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462817 | ||||||
chr11:10462824
|
G | A | 9 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(6): Show | 11 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+1084G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462824 | ||||||
chr11:10462903
|
C | T | 2 | a0001c0004t0001g0285a0001c0004t0001g0288 | 2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.221+1163C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462903 | ||||||
chr11:10463008
|
A | T | 1 | a0003c0008t0009g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.221+1268A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463008 | ||||||
chr11:10463015
|
T | C | 6 | a0001c0001t0022g0184a0001c0003t0005g0128a0001c0003t0005g0129others(3): Show | 6 | HG01943.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+1275T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463015 | ||||||
chr11:10463096
|
C | T | 1 | a0001c0002t0002g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.221+1356C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463096 | ||||||
chr11:10463299
|
G | T | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1559G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463299 | ||||||
chr11:10463451
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+1711G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463451 | ||||||
chr11:10463498
|
G | A | 3 | a0001c0002t0001g0294a0001c0002t0001g0295a0001c0002t0001g0296 | 3 | HG01928.hp2 NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.221+1758G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463498 | ||||||
chr11:10463640
|
A | G | 43 | a0001c0001t0001g0083a0001c0001t0003g0018a0001c0001t0003g0019others(40): Show | 49 | HG00423.hp2 HG00609.hp2 HG02040.hp1 others(46): Show |
intron_variant | MODIFIER | c.221+1900A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463640 | ||||||
chr11:10463837
|
C | T | 1 | a0001c0001t0002g0117 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.221+2097C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463837 | ||||||
chr11:10463852
|
C | A | 358 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.221+2112C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463852 | ||||||
chr11:10463886
|
G | A | 42 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(39): Show | 47 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.221+2146G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463886 | ||||||
chr11:10464243
|
A | G | 3 | a0002c0006t0005g0206a0002c0006t0005g0207a0002c0006t0012g0208 | 3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.221+2503A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464243 | ||||||
chr11:10464571
|
G | A | 1 | a0001c0001t0020g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221+2831G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464571 | ||||||
chr11:10464603
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.221+2863C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464603 | ||||||
chr11:10464626
|
T | C | 297 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.221+2886T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464626 | ||||||
chr11:10464640
|
G | A | 213 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(210): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.221+2900G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464640 | ||||||
chr11:10464707
|
C | T | 128 | a0001c0001t0001g0027a0001c0001t0001g0214a0001c0001t0001g0222others(125): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.221+2967C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464707 | ||||||
chr11:10465271
|
A | T | 30 | a0001c0001t0022g0184a0001c0003t0003g0032a0001c0003t0003g0205others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.221+3531A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465271 | ||||||
chr11:10465284
|
A | G | 3 | a0001c0001t0008g0166a0004c0014t0015g0168a0004c0014t0018g0169 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221+3544A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465284 | ||||||
chr11:10465307
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.221+3567T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465307 | ||||||
chr11:10465351
|
G | A | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.221+3611G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465351 | ||||||
chr11:10465397
|
TA | T | 30 | a0001c0001t0022g0184a0001c0003t0003g0032a0001c0003t0003g0205others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.221+3663delA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10465397 | |||||
chr11:10465410
|
T | C | 10 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(7): Show | 12 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+3670T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465410 | ||||||
chr11:10465474
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+3734G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465474 | ||||||
chr11:10465545
|
C | T | 5 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0002t0029g0118others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+3805C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465545 | ||||||
chr11:10465558
|
A | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+3818A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465558 | ||||||
chr11:10465784
|
C | T | 1 | a0001c0003t0012g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.221+4044C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465784 | ||||||
chr11:10465793
|
A | G | 10 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0330others(7): Show | 11 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+4053A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465793 | ||||||
chr11:10465819
|
G | GT | 62 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0278others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.221+4100dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10465819 | |||||
chr11:10465819
|
GT | G | 13 | a0001c0001t0001g0209a0001c0001t0001g0330a0001c0001t0001g0347others(10): Show | 13 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.221+4100delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10465819 | |||||
chr11:10465988
|
G | A | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.221+4248G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465988 | ||||||
chr11:10466122
|
C | T | 10 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(7): Show | 12 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+4382C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466122 | ||||||
chr11:10466123
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.221+4383G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466123 | ||||||
chr11:10466450
|
C | T | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.221+4710C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466450 | ||||||
chr11:10466466
|
T | C | 355 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(352): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.221+4726T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466466 | ||||||
chr11:10466552
|
T | C | 46 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(43): Show | 51 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.221+4812T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466552 | ||||||
chr11:10466604
|
G | C | 1 | a0001c0001t0003g0139 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.221+4864G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466604 | ||||||
chr11:10466625
|
A | C | 13 | a0001c0001t0008g0166a0001c0003t0004g0003a0001c0003t0004g0023others(10): Show | 15 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.221+4885A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466625 | ||||||
chr11:10466761
|
T | C | 46 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(43): Show | 51 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.221+5021T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466761 | ||||||
chr11:10466865
|
G | C | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+5125G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466865 | ||||||
chr11:10466932
|
C | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+5192C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466932 | ||||||
chr11:10466955
|
G | A | 1 | a0001c0003t0016g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.221+5215G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466955 | ||||||
chr11:10467132
|
G | T | 3 | a0001c0001t0008g0166a0004c0014t0015g0168a0004c0014t0018g0169 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221+5392G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467132 | ||||||
chr11:10467148
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.221+5408A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467148 | ||||||
chr11:10467172
|
C | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+5432C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467172 | ||||||
chr11:10467220
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+5480G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467220 | ||||||
chr11:10467309
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.221+5569A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467309 | ||||||
chr11:10467328
|
C | T | 42 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0330others(39): Show | 43 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.221+5588C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467328 | ||||||
chr11:10467353
|
G | A | 3 | a0001c0001t0027g0231a0001c0002t0001g0232a0001c0013t0011g0178 | 3 | HG03195.hp2 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.221+5613G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467353 | ||||||
chr11:10467395
|
A | G | 10 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(7): Show | 12 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+5655A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467395 | ||||||
chr11:10467535
|
C | T | 1 | a0001c0013t0010g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.221+5795C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467535 | ||||||
chr11:10467685
|
C | T | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.221+5945C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467685 | ||||||
chr11:10467771
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+6031G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467771 | ||||||
chr11:10467881
|
G | T | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.221+6141G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467881 | ||||||
chr11:10468084
|
C | G | 44 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(41): Show | 49 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.221+6344C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468084 | ||||||
chr11:10468252
|
T | C | 1 | a0001c0003t0003g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.221+6512T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468252 | ||||||
chr11:10468279
|
A | C | 86 | a0001c0001t0001g0293a0001c0001t0001g0330a0001c0001t0001g0347others(83): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.221+6539A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468279 | ||||||
chr11:10468280
|
G | T | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+6540G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468280 | ||||||
chr11:10468311
|
G | A | 38 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0127others(35): Show | 42 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.221+6571G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468311 | ||||||
chr11:10468334
|
A | T | 3 | a0001c0003t0004g0023a0001c0003t0004g0173a0004c0015t0007g0174 | 4 | HG02896.hp2 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+6594A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468334 | ||||||
chr11:10468343
|
G | GA | 159 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(156): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.221+6615dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10468343 | |||||
chr11:10468361
|
A | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0274 | 2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.221+6621A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468361 | ||||||
chr11:10468597
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.221+6857A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468597 | ||||||
chr11:10468681
|
G | A | 1 | a0001c0001t0025g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.221+6941G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468681 | ||||||
chr11:10468724
|
T | C | 35 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0235others(32): Show | 37 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.221+6984T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468724 | ||||||
chr11:10468868
|
T | C | 156 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(153): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.221+7128T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468868 | ||||||
chr11:10469164
|
G | C | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+7424G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469164 | ||||||
chr11:10469343
|
T | C | 45 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(42): Show | 50 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.221+7603T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469343 | ||||||
chr11:10469349
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.221+7609C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469349 | ||||||
chr11:10469375
|
C | A | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221+7635C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469375 | ||||||
chr11:10469376
|
A | C | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221+7636A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469376 | ||||||
chr11:10469388
|
A | C | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+7648A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469388 | ||||||
chr11:10469401
|
T | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+7661T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469401 | ||||||
chr11:10469412
|
C | T | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+7672C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469412 | ||||||
chr11:10469418
|
T | C | 296 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.221+7678T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469418 | ||||||
chr11:10469419
|
G | A | 1 | a0001c0001t0020g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221+7679G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469419 | ||||||
chr11:10469551
|
A | G | 1 | a0001c0002t0003g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.221+7811A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469551 | ||||||
chr11:10469552
|
A | C | 45 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(42): Show | 50 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.221+7812A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469552 | ||||||
chr11:10469698
|
A | G | 1 | a0005c0017t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221+7958A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469698 | ||||||
chr11:10469758
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8018G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469758 | ||||||
chr11:10469762
|
G | A | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.221+8022G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469762 | ||||||
chr11:10469766
|
G | A | 1 | a0001c0003t0017g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221+8026G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469766 | ||||||
chr11:10469767
|
C | T | 9 | a0001c0001t0022g0184a0001c0003t0003g0032a0001c0003t0003g0205others(6): Show | 10 | HG00741.hp1 HG01943.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+8027C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469767 | ||||||
chr11:10469810
|
C | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0222a0001c0001t0001g0225others(128): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.221+8070C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469810 | ||||||
chr11:10469815
|
A | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8075A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469815 | ||||||
chr11:10469857
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8117G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469857 | ||||||
chr11:10469897
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.221+8157G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469897 | ||||||
chr11:10469902
|
TAGTGGCG others(5): Show |
T | 9 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(6): Show | 11 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+8163_221+8174d others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469902 | ||||||
chr11:10469909
|
G | A | 1 | a0001c0001t0016g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.221+8169G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469909 | ||||||
chr11:10469957
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8217G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469957 | ||||||
chr11:10469964
|
C | T | 1 | a0001c0002t0003g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.221+8224C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469964 | ||||||
chr11:10469996
|
C | T | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 5 | HG00140.hp2 HG00738.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+8256C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469996 | ||||||
chr11:10469997
|
G | A | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+8257G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469997 | ||||||
chr11:10470026
|
C | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0007g0348 | 3 | HG02451.hp1 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.221+8286C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470026 | ||||||
chr11:10470039
|
C | CA | 7 | a0001c0001t0002g0114a0001c0001t0004g0122a0001c0002t0029g0118others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+8317dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10470039 | |||||
chr11:10470039
|
CA | C | 163 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0214others(160): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.221+8317delA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10470039 | |||||
chr11:10470039
|
CAA | C | 6 | a0001c0001t0001g0303a0001c0002t0001g0273a0001c0002t0001g0279others(3): Show | 6 | HG02602.hp1 HG03710.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+8316_221+8317d others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10470039 | |||||
chr11:10470187
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.222-8339C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470187 | ||||||
chr11:10470194
|
A | T | 166 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0214others(163): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.222-8332A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470194 | ||||||
chr11:10470272
|
T | C | 1 | a0001c0002t0001g0233 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.222-8254T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470272 | ||||||
chr11:10470398
|
C | T | 20 | a0001c0003t0005g0181a0001c0003t0005g0182a0001c0003t0005g0192others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-8128C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470398 | ||||||
chr11:10470399
|
T | C | 14 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0002t0001g0026others(11): Show | 15 | HG02155.hp1 NA18941.hp1 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.222-8127T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470399 | ||||||
chr11:10470403
|
G | A | 75 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(72): Show | 82 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.222-8123G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470403 | ||||||
chr11:10470425
|
C | T | 3 | a0002c0006t0005g0206a0002c0006t0005g0207a0002c0006t0012g0208 | 3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-8101C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470425 | ||||||
chr11:10470445
|
G | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(58): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.222-8081G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470445 | ||||||
chr11:10470568
|
A | T | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.222-7958A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470568 | ||||||
chr11:10470751
|
CAAGGGAT others(5): Show |
C | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.222-7774_222-7763d others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470751 | ||||||
chr11:10470773
|
C | G | 24 | a0001c0001t0001g0028a0001c0001t0001g0300a0001c0001t0001g0301others(21): Show | 27 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.222-7753C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470773 | ||||||
chr11:10470842
|
C | T | 1 | a0001c0003t0021g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.222-7684C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470842 | ||||||
chr11:10470849
|
A | G | 1 | a0001c0001t0011g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222-7677A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470849 | ||||||
chr11:10471024
|
A | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-7502A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471024 | ||||||
chr11:10471062
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0326a0001c0001t0024g0302 | 4 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-7464A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471062 | ||||||
chr11:10471082
|
A | C | 51 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(48): Show | 57 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.222-7444A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471082 | ||||||
chr11:10471164
|
C | T | 20 | a0001c0003t0005g0181a0001c0003t0005g0182a0001c0003t0005g0192others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-7362C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471164 | ||||||
chr11:10471174
|
C | G | 1 | a0001c0004t0001g0213 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.222-7352C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471174 | ||||||
chr11:10471281
|
C | CTCCT | 46 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(43): Show | 51 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.222-7243_222-7240d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10471281 | |||||
chr11:10471318
|
T | A | 65 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0043others(62): Show | 73 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.222-7208T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471318 | ||||||
chr11:10471448
|
G | C | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-7078G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471448 | ||||||
chr11:10471462
|
T | C | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-7064T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471462 | ||||||
chr11:10471532
|
G | A | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-6994G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471532 | ||||||
chr11:10471628
|
T | G | 1 | a0001c0002t0001g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.222-6898T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471628 | ||||||
chr11:10471709
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(39): Show | 47 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.222-6817C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471709 | ||||||
chr11:10471774
|
G | T | 32 | a0001c0001t0020g0204a0001c0001t0022g0184a0001c0003t0003g0032others(29): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.222-6752G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471774 | ||||||
chr11:10471806
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-6720G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471806 | ||||||
chr11:10471852
|
G | A | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-6674G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471852 | ||||||
chr11:10471853
|
T | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-6673T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471853 | ||||||
chr11:10471958
|
A | G | 1 | a0001c0002t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.222-6568A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471958 | ||||||
chr11:10472022
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.222-6504T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472022 | ||||||
chr11:10472160
|
A | G | 20 | a0001c0003t0005g0181a0001c0003t0005g0182a0001c0003t0005g0192others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-6366A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472160 | ||||||
chr11:10472224
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.222-6302A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472224 | ||||||
chr11:10472308
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-6218G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472308 | ||||||
chr11:10472401
|
C | T | 1 | a0001c0002t0001g0325 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222-6125C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472401 | ||||||
chr11:10472462
|
G | A | 1 | a0001c0003t0016g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.222-6064G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472462 | ||||||
chr11:10472544
|
G | C | 1 | a0004c0014t0015g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.222-5982G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472544 | ||||||
chr11:10472585
|
A | G | 26 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0300others(23): Show | 29 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.222-5941A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472585 | ||||||
chr11:10472626
|
T | C | 3 | a0001c0001t0008g0166a0004c0014t0015g0168a0004c0014t0018g0169 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.222-5900T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472626 | ||||||
chr11:10472628
|
A | G | 1 | a0008c0022t0001g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.222-5898A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472628 | ||||||
chr11:10472707
|
G | C | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.222-5819G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472707 | ||||||
chr11:10472940
|
G | C | 47 | a0001c0001t0001g0293a0001c0001t0001g0342a0001c0001t0002g0002others(44): Show | 52 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.222-5586G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472940 | ||||||
chr11:10472950
|
G | A | 2 | a0001c0001t0001g0305a0001c0002t0001g0297 | 2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.222-5576G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472950 | ||||||
chr11:10472960
|
C | A | 39 | a0001c0001t0001g0214a0001c0001t0003g0018a0001c0001t0003g0019others(36): Show | 43 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.222-5566C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472960 | ||||||
chr11:10473077
|
C | G | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-5449C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473077 | ||||||
chr11:10473131
|
A | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-5395A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473131 | ||||||
chr11:10473275
|
A | C | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-5251A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473275 | ||||||
chr11:10473402
|
G | C | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0176others(8): Show | 13 | HG01891.hp1 HG02080.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.222-5124G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473402 | ||||||
chr11:10473438
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.222-5088G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473438 | ||||||
chr11:10473621
|
C | T | 3 | a0002c0012t0008g0131a0004c0011t0015g0017a0005c0016t0005g0199 | 4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-4905C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473621 | ||||||
chr11:10473678
|
C | T | 41 | a0001c0001t0001g0214a0001c0001t0001g0342a0001c0001t0002g0113others(38): Show | 45 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.222-4848C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473678 | ||||||
chr11:10473746
|
C | T | 358 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.222-4780C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473746 | ||||||
chr11:10473788
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0004g0029 | 3 | HG00140.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.222-4738G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473788 | ||||||
chr11:10473870
|
A | G | 2 | a0001c0001t0001g0342a0001c0001t0011g0031 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.222-4656A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473870 | ||||||
chr11:10473932
|
C | T | 3 | a0001c0001t0008g0166a0004c0014t0015g0168a0004c0014t0018g0169 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.222-4594C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473932 | ||||||
chr11:10473933
|
G | A | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.222-4593G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473933 | ||||||
chr11:10474172
|
C | T | 42 | a0001c0001t0001g0214a0001c0001t0002g0113a0001c0001t0003g0018others(39): Show | 47 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(44): Show |
intron_variant | MODIFIER | c.222-4354C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474172 | ||||||
chr11:10474261
|
G | A | 1 | a0001c0004t0001g0234 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.222-4265G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474261 | ||||||
chr11:10474448
|
A | C | 1 | a0001c0002t0003g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.222-4078A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474448 | ||||||
chr11:10474582
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.222-3944C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474582 | ||||||
chr11:10474620
|
G | A | 32 | a0001c0001t0020g0204a0001c0001t0022g0184a0001c0003t0003g0032others(29): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.222-3906G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474620 | ||||||
chr11:10474664
|
T | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-3862T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474664 | ||||||
chr11:10474674
|
C | G | 10 | a0001c0001t0020g0204a0001c0001t0022g0184a0001c0003t0003g0032others(7): Show | 11 | HG00741.hp1 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.222-3852C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474674 | ||||||
chr11:10474675
|
G | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0004g0029 | 4 | HG00140.hp2 HG02886.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3851G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474675 | ||||||
chr11:10474782
|
C | T | 1 | a0001c0005t0001g0221 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.222-3744C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474782 | ||||||
chr11:10475119
|
T | C | 1 | a0001c0003t0003g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.222-3407T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475119 | ||||||
chr11:10475634
|
T | A | 4 | a0001c0001t0001g0321a0001c0002t0001g0322a0001c0002t0001g0323others(1): Show | 4 | HG00642.hp1 HG01192.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-2892T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475634 | ||||||
chr11:10475706
|
G | C | 1 | a0001c0001t0003g0139 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.222-2820G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475706 | ||||||
chr11:10475844
|
A | G | 1 | a0001c0002t0001g0054 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.222-2682A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475844 | ||||||
chr11:10475920
|
C | A | 121 | a0001c0001t0001g0027a0001c0001t0001g0055a0001c0001t0001g0222others(118): Show | 127 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.222-2606C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475920 | ||||||
chr11:10476053
|
G | A | 98 | a0001c0001t0001g0027a0001c0001t0001g0222a0001c0001t0001g0225others(95): Show | 104 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.222-2473G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476053 | ||||||
chr11:10476092
|
A | G | 1 | a0001c0001t0001g0351 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222-2434A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476092 | ||||||
chr11:10476098
|
A | G | 1 | a0001c0001t0008g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.222-2428A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476098 | ||||||
chr11:10476112
|
G | C | 28 | a0001c0001t0007g0352a0001c0001t0020g0204a0001c0001t0022g0184others(25): Show | 29 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.222-2414G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476112 | ||||||
chr11:10476254
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.222-2272G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476254 | ||||||
chr11:10476304
|
C | A | 1 | a0001c0002t0001g0281 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.222-2222C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476304 | ||||||
chr11:10476420
|
G | C | 49 | a0001c0001t0002g0015a0001c0001t0002g0100a0001c0001t0002g0101others(46): Show | 55 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.222-2106G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476420 | ||||||
chr11:10476442
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.222-2084C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476442 | ||||||
chr11:10476465
|
G | GT | 139 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0055others(136): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.222-2050dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10476465 | |||||
chr11:10476465
|
G | GTT | 6 | a0001c0001t0001g0222a0003c0008t0009g0197a0003c0008t0009g0198others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-2051_222-2050d others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10476465 | |||||
chr11:10476471
|
T | G | 8 | a0001c0001t0002g0014a0001c0001t0002g0088a0001c0001t0002g0092others(5): Show | 9 | HG00558.hp1 HG02083.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-2055T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476471 | ||||||
chr11:10476473
|
T | G | 32 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0016others(29): Show | 36 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.222-2053T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476473 | ||||||
chr11:10476473
|
T | TG | 4 | a0001c0001t0004g0008a0001c0001t0004g0039a0001c0001t0007g0037others(1): Show | 5 | HG02109.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-2053_222-2052i others(3): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476473 | ||||||
chr11:10476475
|
T | G | 112 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0293others(109): Show | 127 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.222-2051T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476475 | ||||||
chr11:10476475
|
T | TG | 67 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0036others(64): Show | 73 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.222-2051_222-2050i others(3): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476475 | ||||||
chr11:10476477
|
G | T | 2 | a0001c0002t0001g0286a0001c0003t0003g0032 | 2 | HG02257.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.222-2049G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476477 | ||||||
chr11:10476668
|
G | A | 2 | a0001c0001t0011g0031a0005c0017t0001g0341 | 2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.222-1858G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476668 | ||||||
chr11:10476841
|
A | G | 1 | a0001c0002t0001g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222-1685A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476841 | ||||||
chr11:10476923
|
T | TAGCA | 211 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(208): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.222-1602_222-1599d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10476923 | |||||
chr11:10476973
|
C | G | 4 | a0002c0012t0008g0131a0002c0012t0026g0040a0004c0011t0015g0017others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-1553C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476973 | ||||||
chr11:10477490
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.222-1036A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477490 | ||||||
chr11:10477556
|
A | G | 211 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(208): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.222-970A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477556 | ||||||
chr11:10477787
|
G | T | 319 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(316): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.222-739G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477787 | ||||||
chr11:10477889
|
A | G | 1 | a0001c0002t0001g0219 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.222-637A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477889 | ||||||
chr11:10477925
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-601C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477925 | ||||||
chr11:10478157
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0003g0165 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.222-369G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478157 | ||||||
chr11:10478209
|
G | A | 26 | a0001c0001t0022g0184a0001c0003t0002g0091a0001c0003t0003g0032others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.222-317G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478209 | ||||||
chr11:10478340
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0004g0029 | 3 | HG00140.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.222-186G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478340 | ||||||
chr11:10478448
|
G | A | 52 | a0001c0001t0002g0015a0001c0001t0002g0100a0001c0001t0002g0101others(49): Show | 58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.222-78G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478448 | ||||||
chr11:10478509
|
T | C | 39 | a0001c0001t0001g0056a0001c0001t0001g0176a0001c0001t0001g0344others(36): Show | 42 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.222-17T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478509 | ||||||
chr11:10478738
|
G | A | 3 | a0002c0006t0005g0206a0002c0006t0005g0207a0002c0006t0012g0208 | 3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
splice_region_variant&intron_variant | LOW | c.426+8G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478738 | ||||||
chr11:10478746
|
G | C | 9 | a0001c0001t0022g0184a0001c0003t0003g0137a0001c0003t0003g0205others(6): Show | 10 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.426+16G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478746 | ||||||
chr11:10478787
|
T | C | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+57T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478787 | ||||||
chr11:10478882
|
A | C | 2 | a0001c0003t0005g0128a0001c0003t0005g0129 | 2 | HG01943.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.426+152A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478882 | ||||||
chr11:10479100
|
A | G | 4 | a0001c0001t0001g0339a0001c0002t0001g0328a0001c0002t0001g0329others(1): Show | 4 | HG01123.hp2 HG01258.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.426+370A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479100 | ||||||
chr11:10479114
|
G | A | 51 | a0001c0001t0002g0015a0001c0001t0002g0100a0001c0001t0002g0101others(48): Show | 57 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.426+384G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479114 | ||||||
chr11:10479214
|
G | C | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.426+484G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479214 | ||||||
chr11:10479242
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.426+512T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479242 | ||||||
chr11:10479279
|
C | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.426+549C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479279 | ||||||
chr11:10479481
|
A | G | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+751A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479481 | ||||||
chr11:10479619
|
G | A | 10 | a0001c0001t0002g0113a0001c0001t0003g0018a0001c0001t0003g0019others(7): Show | 12 | HG00408.hp1 NA18953.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.426+889G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479619 | ||||||
chr11:10479664
|
C | T | 7 | a0001c0001t0001g0248a0001c0001t0001g0269a0001c0001t0001g0270others(4): Show | 7 | HG01255.hp2 HG01496.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.426+934C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479664 | ||||||
chr11:10479757
|
C | G | 228 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(225): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.426+1027C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479757 | ||||||
chr11:10480230
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.426+1500C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480230 | ||||||
chr11:10480389
|
A | T | 1 | a0008c0022t0001g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.426+1659A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480389 | ||||||
chr11:10480396
|
C | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.426+1666C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480396 | ||||||
chr11:10480402
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0004g0006a0001c0001t0004g0313 | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1661G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480402 | ||||||
chr11:10480511
|
T | TGTATTTA others(27): Show |
7 | a0001c0002t0001g0309a0003c0008t0009g0197a0003c0008t0009g0198others(4): Show | 7 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-1541_427-1508d others(36): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 10480511 | |||||
chr11:10480651
|
G | T | 4 | a0001c0001t0001g0339a0001c0002t0001g0328a0001c0002t0001g0329others(1): Show | 4 | HG01123.hp2 HG01258.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1412G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480651 | ||||||
chr11:10480668
|
C | G | 53 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0100others(50): Show | 59 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.427-1395C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480668 | ||||||
chr11:10480740
|
G | A | 2 | a0001c0004t0001g0285a0001c0004t0001g0288 | 2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.427-1323G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480740 | ||||||
chr11:10480850
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.427-1213G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480850 | ||||||
chr11:10480875
|
A | G | 116 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0028others(113): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.427-1188A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480875 | ||||||
chr11:10480962
|
C | T | 2 | a0001c0001t0001g0305a0001c0002t0001g0297 | 2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.427-1101C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480962 | ||||||
chr11:10480976
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.427-1087G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480976 | ||||||
chr11:10481422
|
C | T | 1 | a0005c0017t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-641C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481422 | ||||||
chr11:10481427
|
T | C | 1 | a0001c0001t0002g0100 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.427-636T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481427 | ||||||
chr11:10481444
|
C | T | 40 | a0001c0003t0002g0091a0001c0003t0003g0032a0001c0003t0003g0137others(37): Show | 44 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.427-619C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481444 | ||||||
chr11:10481666
|
G | A | 2 | a0001c0001t0004g0035a0001c0001t0004g0122 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.427-397G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481666 | ||||||
chr11:10481864
|
G | A | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.427-199G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481864 | ||||||
chr11:10481893
|
G | A | 40 | a0001c0003t0002g0091a0001c0003t0003g0032a0001c0003t0003g0137others(37): Show | 44 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.427-170G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481893 | ||||||
chr11:10481904
|
G | A | 29 | a0001c0003t0002g0091a0001c0003t0003g0032a0001c0003t0003g0137others(26): Show | 31 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.427-159G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481904 | ||||||
chr11:10482334
|
A | G | 358 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.589+109A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482334 | ||||||
chr11:10482461
|
G | T | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.589+236G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482461 | ||||||
chr11:10482520
|
T | C | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+295T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482520 | ||||||
chr11:10482521
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+296C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482521 | ||||||
chr11:10482590
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.589+365C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482590 | ||||||
chr11:10482687
|
ATATATAT | A | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.589+466_589+472del others(7): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 10482687 | |||||
chr11:10482940
|
C | T | 2 | a0001c0001t0001g0235a0001c0002t0001g0244 | 2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.589+715C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482940 | ||||||
chr11:10483086
|
A | T | 9 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(6): Show | 11 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+861A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483086 | ||||||
chr11:10483093
|
A | C | 218 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(215): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.589+868A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483093 | ||||||
chr11:10483204
|
A | G | 252 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(249): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.589+979A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483204 | ||||||
chr11:10483477
|
A | G | 1 | a0001c0001t0003g0160 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.589+1252A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483477 | ||||||
chr11:10483609
|
G | C | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.590-1211G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483609 | ||||||
chr11:10483627
|
C | T | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.590-1193C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483627 | ||||||
chr11:10483646
|
A | C | 41 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0293others(38): Show | 45 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.590-1174A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483646 | ||||||
chr11:10483662
|
C | G | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.590-1158C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483662 | ||||||
chr11:10483790
|
G | A | 52 | a0001c0001t0001g0214a0001c0001t0002g0015a0001c0001t0002g0100others(49): Show | 58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.590-1030G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483790 | ||||||
chr11:10483842
|
A | T | 1 | a0001c0003t0017g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.590-978A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483842 | ||||||
chr11:10483854
|
A | C | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.590-966A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483854 | ||||||
chr11:10483888
|
C | T | 1 | a0001c0002t0006g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.590-932C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483888 | ||||||
chr11:10483911
|
A | G | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.590-909A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483911 | ||||||
chr11:10484013
|
A | G | 1 | a0001c0001t0013g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.590-807A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484013 | ||||||
chr11:10484047
|
G | T | 69 | a0001c0001t0001g0083a0001c0001t0001g0209a0001c0001t0001g0210others(66): Show | 77 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.590-773G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484047 | ||||||
chr11:10484149
|
A | G | 10 | a0001c0001t0002g0002a0001c0001t0002g0110a0001c0001t0002g0111others(7): Show | 12 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.590-671A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484149 | ||||||
chr11:10484171
|
A | C | 26 | a0001c0003t0002g0091a0001c0003t0003g0032a0001c0003t0003g0137others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.590-649A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484171 | ||||||
chr11:10484379
|
C | T | 2 | a0001c0001t0001g0305a0001c0002t0001g0297 | 2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.590-441C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484379 | ||||||
chr11:10484395
|
G | A | 52 | a0001c0001t0001g0214a0001c0001t0002g0015a0001c0001t0002g0100others(49): Show | 58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.590-425G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484395 | ||||||
chr11:10484410
|
T | C | 1 | a0001c0002t0001g0026 | 2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.590-410T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484410 | ||||||
chr11:10484467
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.590-353G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484467 | ||||||
chr11:10484488
|
A | G | 342 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(339): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.590-332A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484488 | ||||||
chr11:10484647
|
A | G | 5 | a0001c0001t0001g0268a0001c0001t0003g0019a0001c0001t0003g0136others(2): Show | 6 | NA18967.hp1 NA18969.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-173A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484647 | ||||||
chr11:10484708
|
G | T | 212 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(209): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.590-112G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484708 | ||||||
chr11:10484712
|
A | G | 342 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(339): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.590-108A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484712 | ||||||
chr11:10484741
|
G | T | 1 | a0001c0001t0002g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.590-79G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484741 | ||||||
chr11:10484750
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-70C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484750 | ||||||
chr11:10485072
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.809+33G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485072 | ||||||
chr11:10485127
|
G | C | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+88G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485127 | ||||||
chr11:10485137
|
T | C | 2 | a0001c0001t0002g0094a0001c0001t0002g0097 | 2 | NA19063.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.809+98T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485137 | ||||||
chr11:10485160
|
C | T | 249 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(246): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.809+121C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485160 | ||||||
chr11:10485162
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.809+123C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485162 | ||||||
chr11:10485253
|
T | C | 342 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(339): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.809+214T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485253 | ||||||
chr11:10485309
|
C | A | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+270C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485309 | ||||||
chr11:10485332
|
T | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0088a0001c0001t0002g0093 | 4 | HG00558.hp1 NA18974.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+293T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485332 | ||||||
chr11:10485393
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+354C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485393 | ||||||
chr11:10485405
|
G | C | 59 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0214others(56): Show | 65 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.809+366G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485405 | ||||||
chr11:10485432
|
C | T | 2 | a0001c0013t0010g0175a0001c0013t0011g0178 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.809+393C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485432 | ||||||
chr11:10485557
|
C | T | 1 | a0001c0003t0007g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.809+518C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485557 | ||||||
chr11:10485706
|
C | T | 32 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(29): Show | 36 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.809+667C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485706 | ||||||
chr11:10485765
|
T | TTGCTCAT others(18): Show |
6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+732_809+756dup others(25): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 10485765 | |||||
chr11:10485780
|
G | A | 342 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(339): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.809+741G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485780 | ||||||
chr11:10485796
|
G | A | 16 | a0001c0001t0001g0056a0001c0001t0001g0176a0001c0001t0001g0344others(13): Show | 17 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.809+757G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485796 | ||||||
chr11:10486001
|
G | GTC | 93 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0214others(90): Show | 103 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.809+965_809+966dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 10486001 | |||||
chr11:10486006
|
G | C | 341 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(338): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.809+967G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486006 | ||||||
chr11:10486099
|
C | T | 119 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0076others(116): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.809+1060C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486099 | ||||||
chr11:10486208
|
C | T | 3 | a0001c0001t0001g0315a0001c0001t0004g0006a0001c0001t0004g0313 | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.810-1027C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486208 | ||||||
chr11:10486251
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0344a0001c0001t0004g0035others(6): Show | 10 | HG02080.hp2 HG02145.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.810-984G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486251 | ||||||
chr11:10486434
|
A | G | 99 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0214others(96): Show | 109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.810-801A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486434 | ||||||
chr11:10486541
|
G | C | 1 | a0001c0002t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.810-694G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486541 | ||||||
chr11:10486603
|
A | G | 358 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.810-632A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486603 | ||||||
chr11:10486632
|
C | T | 1 | a0001c0003t0003g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.810-603C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486632 | ||||||
chr11:10486665
|
G | A | 1 | a0001c0002t0001g0009 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.810-570G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486665 | ||||||
chr11:10486797
|
A | C | 2 | a0001c0003t0003g0205a0001c0003t0021g0200 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.810-438A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486797 | ||||||
chr11:10486820
|
T | A | 54 | a0001c0001t0001g0214a0001c0001t0002g0015a0001c0001t0002g0100others(51): Show | 60 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.810-415T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486820 | ||||||
chr11:10486848
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-387C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486848 | ||||||
chr11:10486861
|
C | G | 307 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(304): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.810-374C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486861 | ||||||
chr11:10487017
|
T | C | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-218T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10487017 | ||||||
chr11:10487119
|
G | A | 1 | a0001c0001t0008g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.810-116G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10487119 | ||||||
chr11:10487391
|
T | C | 97 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0214others(94): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.939+27T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487391 | ||||||
chr11:10487468
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0287 | 2 | HG02074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.939+104G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487468 | ||||||
chr11:10487491
|
G | A | 1 | a0001c0003t0005g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.939+127G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487491 | ||||||
chr11:10487646
|
G | C | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+282G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487646 | ||||||
chr11:10487797
|
G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.939+433G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487797 | ||||||
chr11:10487853
|
G | C | 235 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(232): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.939+489G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487853 | ||||||
chr11:10488010
|
GA | G | 10 | a0001c0001t0001g0056a0001c0001t0001g0176a0001c0001t0001g0344others(7): Show | 11 | HG02080.hp2 HG02145.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.939+658delA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 10488010 | |||||
chr11:10488125
|
C | T | 13 | a0001c0001t0001g0036a0001c0001t0004g0047a0001c0003t0003g0032others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+761C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488125 | ||||||
chr11:10488219
|
T | G | 9 | a0001c0001t0002g0015a0001c0001t0002g0100a0001c0001t0002g0101others(6): Show | 10 | HG00558.hp2 NA18942.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.939+855T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488219 | ||||||
chr11:10488349
|
T | C | 1 | a0002c0006t0005g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.939+985T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488349 | ||||||
chr11:10488371
|
G | A | 1 | a0001c0002t0006g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.939+1007G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488371 | ||||||
chr11:10488466
|
TGAGAGAG others(2): Show |
T | 164 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(161): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.939+1112_939+1120d others(11): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 10488466 | |||||
chr11:10488499
|
A | G | 161 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(158): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.939+1135A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488499 | ||||||
chr11:10488501
|
A | G | 308 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(305): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.939+1137A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488501 | ||||||
chr11:10488517
|
T | C | 296 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(293): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.939+1153T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488517 | ||||||
chr11:10488605
|
A | C | 198 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(195): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.939+1241A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488605 | ||||||
chr11:10488612
|
G | T | 132 | a0001c0001t0001g0078a0001c0001t0001g0214a0001c0001t0001g0222others(129): Show | 140 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.939+1248G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488612 | ||||||
chr11:10488634
|
G | T | 4 | a0001c0001t0001g0076a0001c0002t0001g0294a0001c0002t0001g0295others(1): Show | 4 | HG01928.hp2 HG01975.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+1270G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488634 | ||||||
chr11:10488693
|
C | T | 1 | a0001c0003t0014g0007 | 2 | HG00741.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.939+1329C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488693 | ||||||
chr11:10488725
|
T | C | 236 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(233): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.939+1361T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488725 | ||||||
chr11:10489276
|
C | T | 1 | a0001c0001t0016g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+1912C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489276 | ||||||
chr11:10489341
|
G | C | 1 | a0001c0002t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.939+1977G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489341 | ||||||
chr11:10489470
|
G | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0337a0001c0001t0001g0351 | 3 | HG02615.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.939+2106G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489470 | ||||||
chr11:10489595
|
C | T | 49 | a0001c0001t0001g0210a0001c0001t0001g0293a0001c0001t0001g0318others(46): Show | 55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.939+2231C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489595 | ||||||
chr11:10489685
|
C | CT | 26 | a0001c0001t0001g0210a0001c0001t0001g0330a0001c0001t0001g0342others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.939+2333dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 10489685 | |||||
chr11:10489771
|
C | T | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.939+2407C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489771 | ||||||
chr11:10489805
|
C | T | 59 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0086others(56): Show | 64 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.939+2441C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489805 | ||||||
chr11:10490034
|
C | A | 1 | a0001c0003t0016g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.939+2670C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490034 | ||||||
chr11:10490060
|
G | A | 1 | a0001c0002t0001g0283 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.939+2696G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490060 | ||||||
chr11:10490125
|
C | T | 1 | a0001c0001t0003g0149 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.939+2761C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490125 | ||||||
chr11:10490152
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.939+2788G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490152 | ||||||
chr11:10490204
|
C | T | 2 | a0001c0001t0001g0351a0001c0003t0014g0007 | 3 | HG00741.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.939+2840C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490204 | ||||||
chr11:10490426
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.940-2923C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490426 | ||||||
chr11:10490611
|
C | A | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-2738C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490611 | ||||||
chr11:10490761
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-2588C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490761 | ||||||
chr11:10490817
|
C | A | 1 | a0001c0001t0003g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.940-2532C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490817 | ||||||
chr11:10490840
|
C | T | 20 | a0001c0001t0001g0303a0001c0001t0001g0319a0001c0001t0001g0321others(17): Show | 21 | HG00642.hp1 HG01081.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.940-2509C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490840 | ||||||
chr11:10491072
|
C | T | 2 | a0001c0001t0001g0264a0001c0002t0001g0263 | 2 | HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.940-2277C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491072 | ||||||
chr11:10491081
|
G | A | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-2268G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491081 | ||||||
chr11:10491098
|
C | A | 2 | a0001c0003t0002g0091a0001c0003t0017g0186 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.940-2251C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491098 | ||||||
chr11:10491129
|
C | T | 1 | a0001c0002t0001g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.940-2220C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491129 | ||||||
chr11:10491130
|
G | A | 1 | a0001c0001t0002g0014 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.940-2219G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491130 | ||||||
chr11:10491135
|
G | A | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-2214G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491135 | ||||||
chr11:10491147
|
G | T | 1 | a0001c0007t0002g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.940-2202G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491147 | ||||||
chr11:10491152
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.940-2197C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491152 | ||||||
chr11:10491222
|
C | T | 1 | a0001c0003t0017g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940-2127C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491222 | ||||||
chr11:10491473
|
G | A | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-1876G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491473 | ||||||
chr11:10491563
|
A | G | 1 | a0001c0002t0006g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.940-1786A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491563 | ||||||
chr11:10491770
|
A | C | 283 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(280): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.940-1579A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491770 | ||||||
chr11:10491959
|
G | A | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-1390G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491959 | ||||||
chr11:10492002
|
C | T | 7 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(4): Show | 9 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.940-1347C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492002 | ||||||
chr11:10492008
|
C | T | 2 | a0001c0001t0016g0130a0001c0013t0011g0178 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.940-1341C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492008 | ||||||
chr11:10492195
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1154T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492195 | ||||||
chr11:10492209
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1140G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492209 | ||||||
chr11:10492216
|
C | A | 2 | a0001c0003t0003g0205a0001c0003t0021g0200 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.940-1133C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492216 | ||||||
chr11:10492216
|
C | T | 2 | a0001c0001t0016g0130a0001c0013t0011g0178 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.940-1133C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492216 | ||||||
chr11:10492218
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1131T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492218 | ||||||
chr11:10492219
|
G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1130G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492219 | ||||||
chr11:10492222
|
A | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1127A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492222 | ||||||
chr11:10492223
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1126T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492223 | ||||||
chr11:10492224
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1125G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492224 | ||||||
chr11:10492226
|
G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1123G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492226 | ||||||
chr11:10492228
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1121G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492228 | ||||||
chr11:10492236
|
C | CAACACTG others(5): Show |
1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1113_940-1112i others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492236 | ||||||
chr11:10492237
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1112T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492237 | ||||||
chr11:10492247
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1102G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492247 | ||||||
chr11:10492248
|
T | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1101T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492248 | ||||||
chr11:10492255
|
C | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1094C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492255 | ||||||
chr11:10492256
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1093T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492256 | ||||||
chr11:10492257
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1092G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492257 | ||||||
chr11:10492259
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1090T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492259 | ||||||
chr11:10492275
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1074T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492275 | ||||||
chr11:10492278
|
G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1071G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492278 | ||||||
chr11:10492280
|
T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1069T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492280 | ||||||
chr11:10492337
|
G | A | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-1012G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492337 | ||||||
chr11:10492340
|
T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1009T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492340 | ||||||
chr11:10492385
|
T | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-964T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492385 | ||||||
chr11:10492449
|
T | C | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-900T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492449 | ||||||
chr11:10492483
|
A | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-866A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492483 | ||||||
chr11:10492485
|
G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-864G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492485 | ||||||
chr11:10492487
|
T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-862T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492487 | ||||||
chr11:10492491
|
A | G | 1 | a0002c0024t0010g0042 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.940-858A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492491 | ||||||
chr11:10492492
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-857G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492492 | ||||||
chr11:10492493
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-856G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492493 | ||||||
chr11:10492494
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-855G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492494 | ||||||
chr11:10492495
|
T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-854T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492495 | ||||||
chr11:10492497
|
C | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-852C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492497 | ||||||
chr11:10492499
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-850G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492499 | ||||||
chr11:10492501
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-848G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492501 | ||||||
chr11:10492503
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-846G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492503 | ||||||
chr11:10492504
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-845G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492504 | ||||||
chr11:10492505
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-844G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492505 | ||||||
chr11:10492506
|
A | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-843A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492506 | ||||||
chr11:10492507
|
T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-842T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492507 | ||||||
chr11:10492510
|
A | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-839A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492510 | ||||||
chr11:10492512
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-837G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492512 | ||||||
chr11:10492513
|
G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-836G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492513 | ||||||
chr11:10492514
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-835G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492514 | ||||||
chr11:10492515
|
A | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-834A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492515 | ||||||
chr11:10492579
|
A | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-770A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492579 | ||||||
chr11:10492583
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-766T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492583 | ||||||
chr11:10492584
|
G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-765G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492584 | ||||||
chr11:10492713
|
G | A | 41 | a0001c0001t0001g0210a0001c0001t0001g0284a0001c0001t0001g0293others(38): Show | 47 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.940-636G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492713 | ||||||
chr11:10493053
|
C | G | 3 | a0001c0001t0001g0209a0001c0003t0005g0128a0001c0003t0005g0129 | 3 | HG01943.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.940-296C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493053 | ||||||
chr11:10493104
|
C | G | 3 | a0001c0001t0020g0204a0001c0003t0003g0205a0001c0003t0021g0200 | 3 | HG01891.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.940-245C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493104 | ||||||
chr11:10493160
|
A | G | 24 | a0001c0001t0001g0284a0001c0001t0001g0293a0001c0001t0001g0318others(21): Show | 29 | HG00140.hp2 HG00639.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.940-189A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493160 | ||||||
chr11:10493179
|
C | G | 6 | a0001c0001t0001g0209a0001c0003t0005g0128a0001c0003t0005g0129others(3): Show | 6 | HG01943.hp2 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-170C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493179 | ||||||
chr11:10493221
|
A | G | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-128A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493221 | ||||||
chr11:10493269
|
C | T | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.940-80C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493269 | ||||||
chr11:10493756
|
G | A | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+213G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493756 | ||||||
chr11:10493815
|
A | G | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+272A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493815 | ||||||
chr11:10493938
|
A | G | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+395A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493938 | ||||||
chr11:10493944
|
G | A | 1 | a0001c0002t0001g0224 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1134+401G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493944 | ||||||
chr11:10494115
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1134+572G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494115 | ||||||
chr11:10494124
|
C | G | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+581C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494124 | ||||||
chr11:10494154
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0005g0190a0001c0001t0013g0041others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1134+611A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494154 | ||||||
chr11:10494162
|
A | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0278 | 2 | HG02135.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1134+619A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494162 | ||||||
chr11:10494216
|
C | T | 4 | a0004c0011t0015g0017a0004c0014t0015g0168a0004c0014t0018g0169others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+673C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494216 | ||||||
chr11:10494217
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0123 | 2 | HG00733.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1134+674G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494217 | ||||||
chr11:10494246
|
A | G | 49 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(46): Show | 52 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1135-653A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494246 | ||||||
chr11:10494397
|
A | G | 1 | a0001c0002t0001g0256 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1135-502A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494397 | ||||||
chr11:10494509
|
C | CA | 258 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(255): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1135-382dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 10494509 | |||||
chr11:10494597
|
A | G | 1 | a0001c0001t0025g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-302A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494597 | ||||||
chr11:10494656
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1135-243G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494656 | ||||||
chr11:10494672
|
G | A | 14 | a0001c0003t0003g0137a0001c0003t0012g0187a0001c0003t0017g0188others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1135-227G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494672 | ||||||
chr11:10494799
|
G | A | 11 | a0001c0003t0003g0137a0002c0006t0005g0206a0002c0006t0005g0207others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135-100G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494799 | ||||||
chr11:10494829
|
A | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-70A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494829 | ||||||
chr11:10494831
|
G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-68G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494831 | ||||||
chr11:10494832
|
T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-67T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494832 | ||||||
chr11:10494867
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1135-32G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494867 | ||||||
chr11:10494872
|
G | A | 9 | a0001c0001t0001g0209a0001c0001t0004g0035a0001c0003t0005g0128others(6): Show | 9 | HG01891.hp1 HG01943.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1135-27G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494872 | ||||||
chr11:10495135
|
G | C | 4 | a0002c0006t0005g0206a0002c0006t0005g0207a0002c0006t0012g0208others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+105G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495135 | ||||||
chr11:10495199
|
C | T | 8 | a0002c0006t0005g0206a0002c0006t0005g0207a0002c0006t0012g0208others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+169C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495199 | ||||||
chr11:10495287
|
T | A | 21 | a0001c0001t0001g0055a0001c0001t0001g0331a0001c0001t0001g0332others(18): Show | 21 | HG01109.hp2 HG01123.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1266+257T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495287 | ||||||
chr11:10495447
|
G | C | 27 | a0001c0001t0001g0209a0001c0001t0016g0130a0001c0003t0005g0128others(24): Show | 28 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1267-123G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495447 | ||||||
chr11:10495492
|
C | T | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-78C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495492 | ||||||
chr11:10495902
|
A | G | 1 | a0003c0008t0009g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1430+169A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10495902 | ||||||
chr11:10495916
|
C | CT | 50 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(47): Show | 53 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1430+201dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 10495916 | |||||
chr11:10495916
|
CT | C | 25 | a0001c0001t0001g0078a0001c0001t0001g0260a0001c0001t0001g0333others(22): Show | 26 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1430+201delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 10495916 | |||||
chr11:10495935
|
G | T | 51 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(48): Show | 54 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1430+202G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10495935 | ||||||
chr11:10496105
|
T | A | 2 | a0001c0001t0001g0264a0001c0002t0001g0263 | 2 | HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1430+372T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496105 | ||||||
chr11:10496114
|
A | G | 6 | a0003c0008t0009g0197a0003c0008t0009g0198a0003c0008t0019g0167others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1430+381A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496114 | ||||||
chr11:10496151
|
G | A | 2 | a0001c0002t0001g0013a0001c0002t0001g0309 | 3 | HG02080.hp2 HG02155.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1430+418G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496151 | ||||||
chr11:10496329
|
C | T | 1 | a0001c0003t0005g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1431-483C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496329 | ||||||
chr11:10496411
|
C | T | 1 | a0001c0001t0016g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1431-401C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496411 | ||||||
chr11:10496555
|
C | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0330others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1431-257C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496555 | ||||||
chr11:10496704
|
G | C | 44 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0043others(41): Show | 47 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1431-108G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496704 | ||||||
chr11:10496742
|
T | C | 263 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0036others(260): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1431-70T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496742 | ||||||
chr11:10496791
|
C | T | 2 | a0005c0016t0005g0199a0005c0017t0001g0341 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1431-21C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496791 | ||||||
chr11:10496974
|
C | T | 196 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0081others(193): Show | 215 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1557+36C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10496974 | ||||||
chr11:10496995
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1557+57C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10496995 | ||||||
chr11:10497038
|
A | G | 103 | a0001c0001t0001g0072a0001c0001t0001g0225a0001c0001t0001g0230others(100): Show | 112 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1557+100A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497038 | ||||||
chr11:10497068
|
G | A | 13 | a0001c0001t0001g0260a0001c0001t0001g0347a0001c0001t0007g0352others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+130G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497068 | ||||||
chr11:10497292
|
G | GT | 164 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0036others(161): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1557+363dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10497292 | |||||
chr11:10497311
|
A | G | 16 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0326others(13): Show | 17 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1557+373A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497311 | ||||||
chr11:10497313
|
A | G | 99 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0056others(96): Show | 106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1557+375A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497313 | ||||||
chr11:10497338
|
C | A | 5 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(2): Show | 7 | HG00639.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1557+400C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497338 | ||||||
chr11:10497349
|
C | T | 320 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(317): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1557+411C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497349 | ||||||
chr11:10497355
|
C | A | 129 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0056others(126): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1557+417C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497355 | ||||||
chr11:10497370
|
A | G | 354 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(351): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1557+432A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497370 | ||||||
chr11:10497430
|
A | G | 240 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(237): Show | 256 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1557+492A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497430 | ||||||
chr11:10497440
|
A | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0210a0001c0001t0003g0153others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+502A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497440 | ||||||
chr11:10497468
|
G | A | 15 | a0001c0001t0001g0044a0001c0001t0001g0315a0001c0001t0001g0342others(12): Show | 15 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+530G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497468 | ||||||
chr11:10497470
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1557+532C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497470 | ||||||
chr11:10497483
|
C | T | 1 | a0001c0010t0009g0180 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1557+545C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497483 | ||||||
chr11:10497491
|
G | A | 1 | a0001c0002t0001g0232 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1557+553G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497491 | ||||||
chr11:10497504
|
C | T | 1 | a0001c0002t0006g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1557+566C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497504 | ||||||
chr11:10497505
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1557+567G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497505 | ||||||
chr11:10497530
|
G | A | 44 | a0001c0001t0001g0056a0001c0001t0001g0287a0001c0001t0001g0303others(41): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1557+592G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497530 | ||||||
chr11:10497533
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0210a0001c0001t0004g0024 | 3 | HG02809.hp2 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1557+595A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497533 | ||||||
chr11:10497541
|
G | C | 57 | a0001c0001t0001g0028a0001c0001t0001g0043a0001c0001t0001g0046others(54): Show | 62 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1557+603G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497541 | ||||||
chr11:10497602
|
A | G | 4 | a0001c0002t0006g0052a0001c0002t0006g0053a0003c0008t0009g0197others(1): Show | 4 | HG01123.hp1 HG01167.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+664A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497602 | ||||||
chr11:10497604
|
A | G | 4 | a0001c0002t0006g0052a0001c0002t0006g0053a0003c0008t0009g0197others(1): Show | 4 | HG01123.hp1 HG01167.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+666A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497604 | ||||||
chr11:10497700
|
T | A | 63 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0044others(60): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1557+762T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497700 | ||||||
chr11:10497769
|
A | G | 176 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0043others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1557+831A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497769 | ||||||
chr11:10497772
|
G | A | 1 | a0001c0001t0004g0029 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1557+834G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497772 | ||||||
chr11:10497808
|
G | A | 1 | a0001c0003t0014g0007 | 2 | HG00741.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1557+870G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497808 | ||||||
chr11:10497833
|
G | A | 1 | a0001c0003t0012g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1557+895G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497833 | ||||||
chr11:10497871
|
G | A | 11 | a0001c0001t0001g0036a0001c0001t0001g0176a0001c0001t0001g0349others(8): Show | 12 | HG00639.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557+933G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497871 | ||||||
chr11:10497926
|
G | A | 12 | a0001c0001t0007g0037a0001c0001t0010g0038a0001c0003t0007g0172others(9): Show | 13 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+988G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497926 | ||||||
chr11:10497926
|
G | C | 2 | a0001c0001t0001g0078a0001c0001t0002g0102 | 2 | NA19054.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1557+988G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497926 | ||||||
chr11:10498006
|
A | G | 1 | a0001c0001t0007g0352 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1557+1068A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498006 | ||||||
chr11:10498077
|
G | A | 1 | a0001c0003t0005g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1557+1139G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498077 | ||||||
chr11:10498091
|
T | C | 2 | a0001c0001t0004g0029a0001c0003t0002g0091 | 3 | HG01243.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1557+1153T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498091 | ||||||
chr11:10498135
|
G | A | 2 | a0001c0001t0001g0067a0001c0002t0001g0346 | 2 | HG01168.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1557+1197G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498135 | ||||||
chr11:10498269
|
G | T | 9 | a0001c0001t0008g0157a0001c0001t0010g0038a0001c0003t0005g0193others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+1331G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498269 | ||||||
chr11:10498323
|
G | A | 14 | a0001c0001t0004g0006a0001c0001t0004g0008a0001c0001t0004g0010others(11): Show | 18 | HG00639.hp2 HG01106.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1557+1385G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498323 | ||||||
chr11:10498349
|
A | G | 8 | a0001c0001t0008g0157a0001c0001t0010g0038a0001c0003t0012g0189others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+1411A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498349 | ||||||
chr11:10498395
|
G | T | 8 | a0001c0001t0007g0348a0001c0001t0007g0353a0001c0003t0012g0187others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+1457G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498395 | ||||||
chr11:10498402
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0004g0024 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1557+1464C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498402 | ||||||
chr11:10498489
|
G | C | 48 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0070others(45): Show | 51 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1557+1551G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498489 | ||||||
chr11:10498651
|
T | C | 1 | a0001c0002t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1558-1435T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498651 | ||||||
chr11:10498729
|
T | C | 348 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(345): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1558-1357T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498729 | ||||||
chr11:10498824
|
A | G | 3 | a0001c0001t0001g0303a0001c0001t0002g0110a0001c0002t0006g0064 | 3 | HG01358.hp2 HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1558-1262A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498824 | ||||||
chr11:10498857
|
C | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0023a0001c0003t0004g0170others(3): Show | 8 | HG00639.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-1229C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498857 | ||||||
chr11:10498888
|
T | C | 3 | a0001c0002t0001g0048a0001c0003t0004g0177a0001c0013t0011g0178 | 3 | HG03130.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1558-1198T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498888 | ||||||
chr11:10498980
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0002g0100 | 2 | NA18966.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1558-1106G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498980 | ||||||
chr11:10499025
|
AGAGG | A | 45 | a0001c0001t0001g0036a0001c0001t0001g0222a0001c0001t0001g0225others(42): Show | 47 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.1558-1059_1558-105 others(8): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10499025 | |||||
chr11:10499028
|
G | C | 52 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0070others(49): Show | 55 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1558-1058G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499028 | ||||||
chr11:10499089
|
GCAAGGAC others(3): Show |
G | 9 | a0001c0001t0007g0037a0001c0001t0007g0348a0001c0001t0007g0352others(6): Show | 10 | HG01884.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-995_1558-986d others(12): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10499089 | |||||
chr11:10499109
|
C | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1558-977C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499109 | ||||||
chr11:10499124
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0004g0024a0001c0001t0016g0130others(1): Show | 4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-962C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499124 | ||||||
chr11:10499143
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0004g0024a0001c0001t0016g0130others(1): Show | 4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-943C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499143 | ||||||
chr11:10499175
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1558-911C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499175 | ||||||
chr11:10499234
|
G | GT | 12 | a0001c0001t0008g0022a0001c0001t0008g0138a0001c0001t0008g0157others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1558-844dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10499234 | |||||
chr11:10499236
|
T | A | 4 | a0001c0001t0001g0024a0001c0001t0004g0024a0001c0001t0016g0130others(1): Show | 4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-850T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499236 | ||||||
chr11:10499251
|
T | C | 1 | a0001c0001t0010g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1558-835T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499251 | ||||||
chr11:10499276
|
C | A | 52 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0070others(49): Show | 55 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1558-810C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499276 | ||||||
chr11:10499280
|
C | A | 3 | a0001c0002t0001g0048a0001c0003t0004g0177a0001c0013t0011g0178 | 3 | HG03130.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1558-806C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499280 | ||||||
chr11:10499305
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0003g0153others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-781C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499305 | ||||||
chr11:10499362
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1558-724C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499362 | ||||||
chr11:10499517
|
A | T | 1 | a0001c0002t0002g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1558-569A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499517 | ||||||
chr11:10499528
|
T | G | 1 | a0001c0003t0005g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1558-558T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499528 | ||||||
chr11:10499700
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1558-386G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499700 | ||||||
chr11:10499884
|
G | A | 1 | a0005c0016t0005g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1558-202G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499884 | ||||||
chr11:10500025
|
C | T | 20 | a0001c0001t0004g0006a0001c0001t0004g0008a0001c0001t0004g0010others(17): Show | 26 | HG00639.hp2 HG01106.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558-61C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10500025 | ||||||
chr11:10500032
|
G | A | 2 | a0001c0001t0007g0348a0001c0001t0007g0353 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1558-54G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10500032 | ||||||
chr11:10500268
|
C | T | 1 | a0001c0001t0020g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1721+19C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500268 | ||||||
chr11:10500296
|
C | T | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1721+47C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500296 | ||||||
chr11:10500303
|
G | A | 167 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0349others(164): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1721+54G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500303 | ||||||
chr11:10500373
|
T | C | 1 | a0001c0003t0005g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1721+124T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500373 | ||||||
chr11:10500401
|
C | T | 172 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0176others(169): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1721+152C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500401 | ||||||
chr11:10500450
|
C | T | 185 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0176others(182): Show | 204 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1721+201C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500450 | ||||||
chr11:10500453
|
G | C | 9 | a0001c0001t0004g0029a0001c0001t0013g0030a0001c0001t0013g0041others(6): Show | 10 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721+204G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500453 | ||||||
chr11:10500554
|
C | T | 1 | a0001c0003t0003g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1721+305C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500554 | ||||||
chr11:10500573
|
C | T | 170 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0176others(167): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1721+324C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500573 | ||||||
chr11:10500704
|
G | A | 1 | a0001c0002t0001g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1721+455G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500704 | ||||||
chr11:10500737
|
G | A | 9 | a0001c0002t0001g0001a0001c0002t0001g0240a0001c0002t0001g0241others(6): Show | 11 | NA18747.hp1 NA18959.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.1721+488G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500737 | ||||||
chr11:10500779
|
G | A | 9 | a0001c0001t0007g0037a0001c0001t0007g0348a0001c0001t0007g0352others(6): Show | 10 | HG01884.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721+530G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500779 | ||||||
chr11:10500796
|
G | A | 138 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0349others(135): Show | 150 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1721+547G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500796 | ||||||
chr11:10500801
|
C | G | 4 | a0001c0001t0001g0024a0001c0001t0004g0024a0001c0001t0016g0130others(1): Show | 4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721+552C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500801 | ||||||
chr11:10500814
|
C | T | 11 | a0001c0001t0001g0248a0001c0001t0001g0270a0001c0001t0001g0271others(8): Show | 13 | HG01255.hp2 HG01496.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1721+565C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500814 | ||||||
chr11:10500832
|
G | A | 4 | a0001c0003t0017g0188a0002c0020t0018g0152a0004c0014t0018g0169others(1): Show | 4 | HG02055.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721+583G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500832 | ||||||
chr11:10500958
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1722-512C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500958 | ||||||
chr11:10501166
|
G | A | 3 | a0001c0007t0001g0334a0001c0007t0002g0034a0001c0007t0002g0126 | 3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1722-304G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501166 | ||||||
chr11:10501209
|
G | A | 45 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0230others(42): Show | 47 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.1722-261G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501209 | ||||||
chr11:10501247
|
G | A | 1 | a0001c0002t0029g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1722-223G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501247 | ||||||
chr11:10501295
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1722-175C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501295 | ||||||
chr11:10501299
|
A | G | 356 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(353): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1722-171A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501299 | ||||||
chr11:10501322
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1722-148G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501322 | ||||||
chr11:10501383
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1722-87C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501383 | ||||||
chr11:10501413
|
C | T | 9 | a0001c0001t0007g0037a0001c0001t0007g0348a0001c0001t0007g0352others(6): Show | 10 | HG01884.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1722-57C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501413 | ||||||
chr11:10501430
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1722-40G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501430 | ||||||
chr11:10501431
|
G | T | 89 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0044others(86): Show | 95 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1722-39G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501431 | ||||||
chr11:10501436
|
G | T | 172 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0058others(169): Show | 187 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1722-34G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501436 | ||||||
chr11:10501607
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1842+17C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501607 | ||||||
chr11:10501612
|
G | A | 1 | a0001c0003t0014g0007 | 2 | HG00741.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1842+22G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501612 | ||||||
chr11:10501677
|
G | A | 28 | a0001c0001t0004g0006a0001c0001t0004g0008a0001c0001t0004g0010others(25): Show | 35 | HG00639.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1842+87G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501677 | ||||||
chr11:10501926
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1842+336C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501926 | ||||||
chr11:10501929
|
C | T | 287 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1842+339C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501929 | ||||||
chr11:10501954
|
A | G | 52 | a0001c0001t0001g0036a0001c0001t0001g0055a0001c0001t0001g0222others(49): Show | 54 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.1842+364A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501954 | ||||||
chr11:10501972
|
G | A | 147 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0349others(144): Show | 160 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1842+382G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501972 | ||||||
chr11:10501975
|
A | G | 3 | a0001c0001t0008g0157a0001c0001t0010g0038a0001c0013t0010g0175 | 3 | HG02109.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1842+385A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501975 | ||||||
chr11:10502125
|
C | T | 3 | a0001c0002t0001g0229a0001c0004t0001g0234a0001c0005t0001g0221 | 3 | HG02155.hp1 NA18974.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1842+535C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502125 | ||||||
chr11:10502261
|
G | A | 1 | a0001c0002t0003g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1843-460G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502261 | ||||||
chr11:10502398
|
A | G | 2 | a0005c0016t0005g0199a0005c0017t0001g0341 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1843-323A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502398 | ||||||
chr11:10502427
|
T | C | 1 | a0001c0002t0001g0327 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1843-294T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502427 | ||||||
chr11:10502442
|
G | A | 1 | a0001c0001t0025g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1843-279G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502442 | ||||||
chr11:10502532
|
T | A | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1843-189T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502532 | ||||||
chr11:10502627
|
C | G | 1 | a0001c0002t0001g0236 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1843-94C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502627 | ||||||
chr11:10502964
|
G | T | 1 | a0002c0012t0026g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2016+70G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10502964 | ||||||
chr11:10503059
|
C | G | 131 | a0001c0001t0003g0140a0001c0002t0001g0001a0001c0002t0001g0004others(128): Show | 143 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.2016+165C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503059 | ||||||
chr11:10503125
|
A | G | 1 | a0001c0001t0002g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2016+231A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503125 | ||||||
chr11:10503274
|
C | T | 3 | a0001c0001t0001g0209a0001c0003t0005g0128a0001c0003t0005g0129 | 3 | HG01943.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2016+380C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503274 | ||||||
chr11:10503440
|
A | T | 4 | a0001c0001t0001g0225a0001c0001t0003g0149a0001c0001t0003g0163others(1): Show | 4 | NA18940.hp2 NA18952.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2016+546A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503440 | ||||||
chr11:10503554
|
C | A | 1 | a0001c0002t0006g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2016+660C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503554 | ||||||
chr11:10503566
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2016+672G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503566 | ||||||
chr11:10503832
|
A | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0070others(48): Show | 54 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2017-717A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503832 | ||||||
chr11:10504115
|
C | CATCT | 13 | a0001c0001t0001g0055a0001c0001t0001g0225a0001c0001t0001g0293others(10): Show | 14 | HG00558.hp1 HG01515.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017-403_2017-400d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | |||||
chr11:10504115
|
CATCT | C | 7 | a0001c0001t0013g0030a0001c0003t0017g0186a0001c0003t0017g0188others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-403_2017-400d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | |||||
chr11:10504115
|
CATCTATC others(1): Show |
C | 110 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(107): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2017-407_2017-400d others(10): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | |||||
chr11:10504115
|
CATCTATC others(5): Show |
C | 171 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0059others(168): Show | 186 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2017-411_2017-400d others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | |||||
chr11:10504115
|
CATCTATC others(9): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2017-415_2017-400d others(18): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | |||||
chr11:10504160
|
A | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0070others(48): Show | 54 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2017-389A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504160 | ||||||
chr11:10504244
|
A | C | 13 | a0001c0001t0008g0022a0001c0001t0008g0138a0001c0001t0008g0157others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2017-305A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504244 | ||||||
chr11:10504248
|
G | T | 34 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0049others(31): Show | 37 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2017-301G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504248 | ||||||
chr11:10504372
|
A | G | 98 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0044others(95): Show | 108 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.2017-177A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504372 | ||||||
chr11:10504513
|
C | T | 288 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(285): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2017-36C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504513 | ||||||
chr11:10504729
|
A | G | 1 | a0001c0003t0004g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2127+70A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504729 | ||||||
chr11:10504889
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2127+230A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504889 | ||||||
chr11:10504903
|
C | G | 1 | a0001c0002t0001g0296 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2127+244C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504903 | ||||||
chr11:10504908
|
T | G | 2 | a0001c0001t0001g0349a0001c0001t0020g0204 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2127+249T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504908 | ||||||
chr11:10505074
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2127+415C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505074 | ||||||
chr11:10505075
|
G | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0059others(19): Show | 24 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2127+416G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505075 | ||||||
chr11:10505178
|
G | C | 1 | a0001c0002t0001g0246 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2127+519G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505178 | ||||||
chr11:10505279
|
TG | T | 33 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0049others(30): Show | 36 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2128-428delG | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505279 | ||||||
chr11:10505375
|
C | CAGG | 348 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(345): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2128-332_2128-330d others(5): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 10505375 | |||||
chr11:10505380
|
G | A | 348 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(345): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2128-328G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505380 | ||||||
chr11:10505406
|
TC | T | 27 | a0001c0001t0001g0024a0001c0001t0001g0068a0001c0001t0004g0006others(24): Show | 34 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2128-298delC | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 10505406 | |||||
chr11:10505410
|
CT | C | 321 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(318): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.2128-295delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 10505410 | |||||
chr11:10505505
|
AC | A | 139 | a0001c0001t0001g0043a0001c0001t0001g0176a0001c0001t0001g0349others(136): Show | 151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2128-202delC | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505505 | ||||||
chr11:10505597
|
G | A | 1 | a0001c0001t0004g0029 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2128-111G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505597 |