geneid | 132949 |
---|---|
ensemblid | ENSG00000157426.14 |
hgncid | 23993 |
symbol | AASDH |
name | aminoadipate-semialdehyde dehydrogenase |
refseq_nuc | NM_181806.4 |
refseq_prot | NP_861522.2 |
ensembl_nuc | ENST00000205214.11 |
ensembl_prot | ENSP00000205214.6 |
mane_status | MANE Select |
chr | chr4 |
start | 56338290 |
end | 56387491 |
strand | - |
ver | v1.2 |
region | chr4:56338290-56387491 |
region5000 | chr4:56333290-56392491 |
regionname0 | AASDH_chr4_56338290_56387491 |
regionname5000 | AASDH_chr4_56333290_56392491 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1098 | 130 | 26 | 16 | 73 | 8 | 6 | 59 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002 | 0/0 | 1098 | 92 | 16 | 19 | 50 | 2 | 5 | 43 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0003 | 0/1 | 1098 | 77 | 25 | 24 | 6 | 6 | 15 | 3 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0004 | 0/0 | 1098 | 54 | 2 | 0 | 44 | 0 | 8 | 36 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0005 | 0/0 | 1097 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0006 | 0/0 | 1098 | 4 | 3 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0007 | 0/0 | 1098 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0008 | 0/0 | 1098 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0009 | 0/0 | 1098 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0010 | 0/0 | 145 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0011 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0012 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0013 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0014 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0015 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0016 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0017 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0018 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3297 | 87 | 19 | 12 | 46 | 5 | 4 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0002 | 0/0 | 3297 | 82 | 16 | 19 | 40 | 2 | 5 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0003 | 0/1 | 3297 | 77 | 25 | 24 | 6 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0004 | 0/0 | 3297 | 53 | 2 | 0 | 43 | 0 | 8 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0005 | 0/0 | 3297 | 40 | 4 | 4 | 27 | 3 | 2 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0006 | 0/0 | 3297 | 9 | 0 | 0 | 9 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0007 | 0/0 | 3294 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0008 | 0/0 | 3297 | 4 | 4 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0009 | 0/0 | 3297 | 3 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0010 | 0/0 | 3297 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0011 | 0/0 | 3297 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0012 | 0/0 | 3297 | 2 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0013 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0014 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0015 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0016 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0017 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0018 | 0/0 | 3297 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0019 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0020 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0021 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0022 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0023 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0024 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
c0025 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 285 | 289 | 51 | 36 | 170 | 10 | 21 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
t0002 | 0/1 | 289 | 79 | 25 | 24 | 8 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
t0003 | 0/0 | 285 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
t0004 | 0/0 | 285 | 3 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
t0005 | 0/0 | 285 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
t0006 | 0/0 | 285 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
t0007 | 0/0 | 285 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0004 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3297 | 87 | 19 | 12 | 46 | 5 | 4 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0005 | 0/0 | 3297 | 40 | 4 | 4 | 27 | 3 | 2 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0010 | 0/0 | 3297 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0019 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0002 | 0/0 | 3297 | 82 | 16 | 19 | 40 | 2 | 5 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0006 | 0/0 | 3297 | 9 | 0 | 0 | 9 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0024 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0003c0003 | 0/1 | 3297 | 77 | 25 | 24 | 6 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0004c0004 | 0/0 | 3297 | 53 | 2 | 0 | 43 | 0 | 8 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0004c0025 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0005c0007 | 0/0 | 3294 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0006c0009 | 0/0 | 3297 | 3 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0006c0020 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0007c0008 | 0/0 | 3297 | 4 | 4 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0008c0011 | 0/0 | 3297 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0009c0012 | 0/0 | 3297 | 2 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0010c0013 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0011c0014 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0012c0015 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0013c0017 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0014c0016 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0015c0021 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0016c0018 | 0/0 | 3297 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0017c0022 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0018c0023 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3581 | 87 | 19 | 12 | 46 | 5 | 4 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0005t0001 | 0/0 | 3581 | 39 | 4 | 4 | 26 | 3 | 2 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0005t0005 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0010t0001 | 0/0 | 3581 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0001c0019t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0002t0001 | 0/0 | 3581 | 81 | 15 | 19 | 40 | 2 | 5 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0002t0007 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0006t0001 | 0/0 | 3581 | 9 | 0 | 0 | 9 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0002c0024t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0003c0003t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0003c0003t0002 | 0/1 | 3585 | 76 | 24 | 24 | 6 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0004c0004t0001 | 0/0 | 3581 | 52 | 2 | 0 | 42 | 0 | 8 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0004c0004t0006 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0004c0025t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0005c0007t0003 | 0/0 | 3578 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0006c0009t0004 | 0/0 | 3581 | 3 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0006c0020t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0007c0008t0001 | 0/0 | 3581 | 4 | 4 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0008c0011t0002 | 0/0 | 3585 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0009c0012t0001 | 0/0 | 3581 | 2 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0010c0013t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0011c0014t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0012c0015t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0013c0017t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0014c0016t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0015c0021t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0016c0018t0001 | 0/0 | 3581 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0017c0022t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
a0018c0023t0002 | 0/0 | 3585 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | copy fasta | chr4 | 56333290 | 56392491 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0004 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0010t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0010t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0019t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0024t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0025t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0009t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0009t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0020t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0008t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0008t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0008t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0008t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0008c0011t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0008c0011t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0009c0012t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0009c0012t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0010c0013t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0011c0014t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0012c0015t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0013c0017t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0014c0016t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0015c0021t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0016c0018t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0017c0022t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0018c0023t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0001 | g0305 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00140 | hp1 | a0003 | c0003 | t0002 | g0270 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00140 | hp2 | a0003 | c0003 | t0002 | g0260 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00280 | hp1 | a0003 | c0003 | t0002 | g0025 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00280 | hp2 | a0003 | c0003 | t0002 | g0257 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0304 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00323 | hp2 | a0003 | c0003 | t0002 | g0239 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00408 | hp1 | a0004 | c0004 | t0001 | g0172 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00423 | hp1 | a0004 | c0004 | t0001 | g0146 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00423 | hp2 | a0004 | c0004 | t0001 | g0138 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00438 | hp1 | a0004 | c0004 | t0001 | g0139 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00544 | hp1 | a0001 | c0005 | t0001 | g0309 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00609 | hp2 | a0003 | c0003 | t0002 | g0243 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00639 | hp1 | a0003 | c0003 | t0002 | g0271 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00735 | hp1 | a0003 | c0003 | t0002 | g0027 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00738 | hp1 | a0003 | c0003 | t0002 | g0247 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00738 | hp2 | a0003 | c0003 | t0002 | g0277 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00741 | hp1 | a0003 | c0003 | t0002 | g0253 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00741 | hp2 | a0003 | c0003 | t0002 | g0266 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0303 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01070 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01070 | hp2 | a0001 | c0005 | t0001 | g0284 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0010 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0293 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01081 | hp2 | a0003 | c0003 | t0002 | g0025 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0321 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01167 | hp1 | a0003 | c0003 | t0002 | g0265 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01167 | hp2 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0261 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01169 | hp2 | a0003 | c0003 | t0002 | g0328 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01175 | hp2 | a0003 | c0003 | t0002 | g0274 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01243 | hp1 | a0003 | c0003 | t0002 | g0251 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01255 | hp1 | a0003 | c0003 | t0002 | g0327 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01258 | hp1 | a0003 | c0003 | t0002 | g0295 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01261 | hp1 | a0009 | c0012 | t0001 | g0152 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01346 | hp1 | a0003 | c0003 | t0002 | g0027 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01358 | hp1 | a0003 | c0003 | t0002 | g0254 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01433 | hp1 | a0003 | c0003 | t0002 | g0267 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0196 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0301 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0197 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01884 | hp1 | a0005 | c0007 | t0003 | g0033 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0021 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01993 | hp2 | a0003 | c0003 | t0002 | g0010 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02015 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02027 | hp2 | a0001 | c0005 | t0001 | g0051 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02040 | hp1 | a0001 | c0005 | t0001 | g0050 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02055 | hp1 | a0003 | c0003 | t0002 | g0275 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02055 | hp2 | a0003 | c0003 | t0002 | g0262 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02056 | hp1 | a0001 | c0005 | t0001 | g0313 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02056 | hp2 | a0003 | c0003 | t0002 | g0272 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02080 | hp2 | a0004 | c0004 | t0001 | g0135 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02083 | hp1 | a0003 | c0003 | t0002 | g0245 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02129 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02145 | hp1 | a0005 | c0007 | t0003 | g0040 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02145 | hp2 | a0007 | c0008 | t0001 | g0326 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02148 | hp1 | a0003 | c0003 | t0002 | g0294 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CDX | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02257 | hp1 | a0006 | c0009 | t0004 | g0029 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02258 | hp1 | a0003 | c0003 | t0002 | g0045 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02258 | hp2 | a0006 | c0009 | t0004 | g0029 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02293 | hp2 | a0001 | c0005 | t0001 | g0298 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02300 | hp2 | a0003 | c0003 | t0002 | g0297 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0250 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02523 | hp2 | a0004 | c0004 | t0001 | g0145 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02622 | hp1 | a0003 | c0003 | t0002 | g0289 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02622 | hp2 | a0003 | c0003 | t0002 | g0291 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02630 | hp1 | a0005 | c0007 | t0003 | g0038 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0322 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0220 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02717 | hp2 | a0003 | c0003 | t0002 | g0263 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02735 | hp2 | a0003 | c0003 | t0002 | g0026 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02809 | hp1 | a0003 | c0003 | t0002 | g0003 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02809 | hp2 | a0001 | c0010 | t0001 | g0281 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02895 | hp1 | a0014 | c0016 | t0001 | g0218 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02895 | hp2 | a0003 | c0003 | t0002 | g0241 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02896 | hp1 | a0003 | c0003 | t0002 | g0049 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02896 | hp2 | a0003 | c0003 | t0002 | g0003 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02897 | hp1 | a0003 | c0003 | t0002 | g0046 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0240 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02976 | hp1 | a0001 | c0010 | t0001 | g0280 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03041 | hp1 | a0005 | c0007 | t0003 | g0039 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03041 | hp2 | a0007 | c0008 | t0001 | g0059 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03130 | hp1 | a0003 | c0003 | t0002 | g0269 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03130 | hp2 | a0007 | c0008 | t0001 | g0061 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03139 | hp1 | a0005 | c0007 | t0003 | g0037 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03195 | hp1 | a0006 | c0009 | t0004 | g0331 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03195 | hp2 | a0003 | c0003 | t0002 | g0047 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03209 | hp1 | a0003 | c0003 | t0002 | g0052 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03209 | hp2 | a0001 | c0019 | t0001 | g0064 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03225 | hp1 | a0005 | c0007 | t0003 | g0034 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03239 | hp1 | a0003 | c0003 | t0002 | g0278 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03453 | hp1 | a0005 | c0007 | t0003 | g0036 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03453 | hp2 | a0003 | c0003 | t0002 | g0044 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03490 | hp1 | a0003 | c0003 | t0002 | g0279 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0148 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03491 | hp1 | a0003 | c0003 | t0002 | g0249 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03491 | hp2 | a0016 | c0018 | t0001 | g0167 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03492 | hp1 | a0003 | c0003 | t0002 | g0248 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03492 | hp2 | a0004 | c0004 | t0001 | g0137 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03516 | hp1 | a0003 | c0003 | t0002 | g0276 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03516 | hp2 | a0002 | c0002 | t0007 | g0330 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03579 | hp1 | a0003 | c0003 | t0002 | g0048 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03579 | hp2 | a0018 | c0023 | t0002 | g0043 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03654 | hp2 | a0009 | c0012 | t0001 | g0153 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03688 | hp1 | a0001 | c0005 | t0001 | g0308 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03688 | hp2 | a0003 | c0003 | t0002 | g0286 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0130 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03710 | hp2 | a0003 | c0003 | t0002 | g0273 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03831 | hp2 | a0004 | c0004 | t0001 | g0041 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03834 | hp1 | a0001 | c0005 | t0001 | g0319 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0238 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0258 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0132 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04115 | hp1 | a0003 | c0003 | t0002 | g0288 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0296 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04199 | hp1 | a0004 | c0004 | t0001 | g0143 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04204 | hp1 | a0004 | c0004 | t0001 | g0133 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04204 | hp2 | a0003 | c0003 | t0002 | g0259 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0268 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0026 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18522 | hp1 | a0007 | c0008 | t0001 | g0060 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18522 | hp2 | a0003 | c0003 | t0002 | g0042 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18612 | hp2 | a0004 | c0004 | t0001 | g0136 | EAS | CHB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0307 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18939 | hp1 | a0004 | c0025 | t0001 | g0126 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18940 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18941 | hp2 | a0004 | c0004 | t0001 | g0129 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18944 | hp2 | a0001 | c0005 | t0001 | g0285 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18946 | hp2 | a0004 | c0004 | t0006 | g0031 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18947 | hp2 | a0001 | c0005 | t0001 | g0028 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18948 | hp1 | a0004 | c0004 | t0001 | g0147 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18954 | hp2 | a0015 | c0021 | t0001 | g0325 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18957 | hp1 | a0001 | c0005 | t0001 | g0302 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18957 | hp2 | a0004 | c0004 | t0001 | g0224 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18959 | hp1 | a0001 | c0005 | t0001 | g0324 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0149 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18961 | hp1 | a0002 | c0006 | t0001 | g0024 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18961 | hp2 | a0004 | c0004 | t0001 | g0151 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18962 | hp1 | a0001 | c0005 | t0001 | g0316 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18962 | hp2 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18963 | hp1 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18964 | hp2 | a0008 | c0011 | t0002 | g0206 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18966 | hp1 | a0017 | c0022 | t0001 | g0109 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0246 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0169 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18968 | hp2 | a0002 | c0006 | t0001 | g0024 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18969 | hp1 | a0002 | c0024 | t0001 | g0234 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18969 | hp2 | a0004 | c0004 | t0001 | g0142 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18972 | hp1 | a0004 | c0004 | t0001 | g0144 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18977 | hp1 | a0004 | c0004 | t0001 | g0020 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18979 | hp1 | a0006 | c0020 | t0001 | g0092 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18982 | hp1 | a0004 | c0004 | t0001 | g0173 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18982 | hp2 | a0002 | c0006 | t0001 | g0237 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18984 | hp1 | a0004 | c0004 | t0001 | g0222 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18985 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18985 | hp2 | a0001 | c0005 | t0001 | g0032 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18986 | hp1 | a0004 | c0004 | t0001 | g0134 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18986 | hp2 | a0008 | c0011 | t0002 | g0205 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18989 | hp1 | a0003 | c0003 | t0002 | g0287 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18989 | hp2 | a0001 | c0005 | t0001 | g0317 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18992 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18992 | hp2 | a0010 | c0013 | t0001 | g0067 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18994 | hp2 | a0004 | c0004 | t0001 | g0140 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18997 | hp2 | a0012 | c0015 | t0001 | g0194 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18998 | hp2 | a0001 | c0005 | t0001 | g0311 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18999 | hp2 | a0002 | c0006 | t0001 | g0229 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19001 | hp1 | a0004 | c0004 | t0001 | g0223 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19001 | hp2 | a0001 | c0005 | t0001 | g0320 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19002 | hp2 | a0004 | c0004 | t0001 | g0171 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19003 | hp2 | a0004 | c0004 | t0001 | g0141 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19005 | hp1 | a0004 | c0004 | t0001 | g0156 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19007 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19009 | hp2 | a0001 | c0005 | t0001 | g0323 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19010 | hp1 | a0002 | c0006 | t0001 | g0188 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19011 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19011 | hp2 | a0001 | c0005 | t0001 | g0300 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19030 | hp2 | a0003 | c0003 | t0002 | g0290 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19043 | hp1 | a0005 | c0007 | t0003 | g0035 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19055 | hp1 | a0004 | c0004 | t0001 | g0020 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19057 | hp2 | a0004 | c0004 | t0001 | g0127 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19058 | hp2 | a0001 | c0005 | t0001 | g0242 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0244 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19063 | hp1 | a0004 | c0004 | t0001 | g0225 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19064 | hp1 | a0002 | c0006 | t0001 | g0228 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19064 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19066 | hp1 | a0002 | c0006 | t0001 | g0231 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19066 | hp2 | a0004 | c0004 | t0001 | g0154 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19070 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19075 | hp1 | a0001 | c0005 | t0001 | g0318 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19077 | hp1 | a0001 | c0005 | t0001 | g0299 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19077 | hp2 | a0002 | c0006 | t0001 | g0230 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19079 | hp1 | a0001 | c0005 | t0005 | g0030 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19080 | hp2 | a0004 | c0004 | t0001 | g0221 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19081 | hp1 | a0001 | c0005 | t0001 | g0312 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19081 | hp2 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19082 | hp1 | a0001 | c0005 | t0001 | g0310 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19083 | hp2 | a0001 | c0005 | t0001 | g0028 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19084 | hp1 | a0004 | c0004 | t0001 | g0170 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0314 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19085 | hp2 | a0004 | c0004 | t0001 | g0128 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19086 | hp1 | a0002 | c0006 | t0001 | g0236 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19088 | hp1 | a0001 | c0005 | t0001 | g0306 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19091 | hp2 | a0004 | c0004 | t0001 | g0131 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19240 | hp1 | a0013 | c0017 | t0001 | g0211 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19240 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20129 | hp1 | a0003 | c0003 | t0002 | g0003 | AFR | ASW | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20129 | hp2 | a0003 | c0003 | t0002 | g0292 | AFR | ASW | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20805 | hp1 | a0003 | c0003 | t0002 | g0264 | EUR | TSI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20905 | hp1 | a0003 | c0003 | t0002 | g0255 | SAS | GIH | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20905 | hp2 | a0004 | c0004 | t0001 | g0155 | SAS | GIH | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03471 | hp1 | a0003 | c0003 | t0002 | g0256 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03471 | hp2 | a0001 | c0005 | t0001 | g0058 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18955 | hp1 | a0004 | c0004 | t0001 | g0150 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | USA | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20300 | hp2 | a0011 | c0014 | t0001 | g0282 | AFR | USA | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0315 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0002 | g0252 | REF | REF | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338591
|
C | T | 1 | a0013 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3108G>A | p.Met1036Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 3280/3581 | 3108/3297 | 1036/1098 | chr4 | 56338591 | ||
chr4:56338611
|
A | C | 5 | a0002a0006a0012others(2): Show | 99 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(96): Show |
missense_variant | MODERATE | c.3088T>G | p.Tyr1030Asp | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 3260/3581 | 3088/3297 | 1030/1098 | chr4 | 56338611 | ||
chr4:56342905
|
C | T | 1 | a0014 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.2837G>A | p.Cys946Tyr | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/15 | 3009/3581 | 2837/3297 | 946/1098 | chr4 | 56342905 | ||
chr4:56345186
|
T | C | 5 | a0002a0008a0012others(2): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
missense_variant | MODERATE | c.2593A>G | p.Thr865Ala | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/15 | 2765/3581 | 2593/3297 | 865/1098 | chr4 | 56345186 | ||
chr4:56349392
|
T | C | 2 | a0007a0011 | 5 | HG02145.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.2359A>G | p.Ile787Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2531/3581 | 2359/3297 | 787/1098 | chr4 | 56349392 | ||
chr4:56349428
|
T | C | 1 | a0015 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.2323A>G | p.Ile775Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2495/3581 | 2323/3297 | 775/1098 | chr4 | 56349428 | ||
chr4:56349431
|
C | T | 1 | a0012 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.2320G>A | p.Val774Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2492/3581 | 2320/3297 | 774/1098 | chr4 | 56349431 | ||
chr4:56349511
|
G | A | 2 | a0003a0018 | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
missense_variant | MODERATE | c.2240C>T | p.Ala747Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2412/3581 | 2240/3297 | 747/1098 | chr4 | 56349511 | ||
chr4:56349637
|
G | A | 1 | a0009 | 2 | HG01261.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.2114C>T | p.Ala705Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2286/3581 | 2114/3297 | 705/1098 | chr4 | 56349637 | ||
chr4:56349803
|
C | T | 1 | a0016 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1948G>A | p.Asp650Asn | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2120/3581 | 1948/3297 | 650/1098 | chr4 | 56349803 | ||
chr4:56355182
|
T | C | 3 | a0004a0009a0017 | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
missense_variant&splice_region_variant | MODERATE | c.1103A>G | p.Lys368Arg | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/15 | 1275/3581 | 1103/3297 | 368/1098 | chr4 | 56355182 | ||
chr4:56371486
|
C | T | 1 | a0011 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.826G>A | p.Val276Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/15 | 998/3581 | 826/3297 | 276/1098 | chr4 | 56371486 | ||
chr4:56378269
|
GTTC | G | 1 | a0005 | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
conservative_inframe_deletion | MODERATE | c.544_546delGAA | p.Glu182del | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/15 | 718/3581 | 544/3297 | 182/1098 | chr4 | 56378269 | ||
chr4:56378283
|
T | C | 1 | a0018 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.533A>G | p.Glu178Gly | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/15 | 705/3581 | 533/3297 | 178/1098 | chr4 | 56378283 | ||
chr4:56378379
|
C | T | 1 | a0010 | 1 | NA18992.hp2 | stop_gained | HIGH | c.437G>A | p.Trp146* | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/15 | 609/3581 | 437/3297 | 146/1098 | chr4 | 56378379 | ||
chr4:56382550
|
G | C | 2 | a0004a0009 | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
missense_variant | MODERATE | c.278C>G | p.Pro93Arg | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/15 | 450/3581 | 278/3297 | 93/1098 | chr4 | 56382550 | ||
chr4:56384119
|
T | C | 2 | a0004a0009 | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
missense_variant | MODERATE | c.181A>G | p.Ile61Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/15 | 353/3581 | 181/3297 | 61/1098 | chr4 | 56384119 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338750
|
C | T | 1 | a0001c0019 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2949G>A | p.Pro983Pro | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 3121/3581 | 2949/3297 | 983/1098 | chr4 | 56338750 | ||
chr4:56349314
|
G | T | 2 | a0002c0006a0002c0024 | 10 | NA18961.hp1 NA18968.hp2 NA18969.hp1 others(7): Show |
synonymous_variant | LOW | c.2437C>A | p.Arg813Arg | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2609/3581 | 2437/3297 | 813/1098 | chr4 | 56349314 | ||
chr4:56353426
|
G | A | 16 | a0001c0005a0001c0010a0002c0002others(13): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
synonymous_variant | LOW | c.1554C>T | p.Asp518Asp | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/15 | 1726/3581 | 1554/3297 | 518/1098 | chr4 | 56353426 | ||
chr4:56353429
|
G | A | 1 | a0005c0007 | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
synonymous_variant | LOW | c.1551C>T | p.Ile517Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/15 | 1723/3581 | 1551/3297 | 517/1098 | chr4 | 56353429 | ||
chr4:56353447
|
C | T | 8 | a0002c0002a0002c0006a0002c0024others(5): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
synonymous_variant | LOW | c.1533G>A | p.Pro511Pro | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/15 | 1705/3581 | 1533/3297 | 511/1098 | chr4 | 56353447 | ||
chr4:56371517
|
G | A | 2 | a0003c0003a0018c0023 | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
synonymous_variant | LOW | c.795C>T | p.Ser265Ser | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/15 | 967/3581 | 795/3297 | 265/1098 | chr4 | 56371517 | ||
chr4:56371559
|
A | G | 1 | a0004c0025 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.753T>C | p.Leu251Leu | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/15 | 925/3581 | 753/3297 | 251/1098 | chr4 | 56371559 | ||
chr4:56382561
|
C | T | 1 | a0001c0010 | 2 | HG02809.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.267G>A | p.Glu89Glu | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/15 | 439/3581 | 267/3297 | 89/1098 | chr4 | 56382561 | ||
chr4:56382564
|
G | A | 1 | a0002c0024 | 1 | NA18969.hp1 | synonymous_variant | LOW | c.264C>T | p.Ile88Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/15 | 436/3581 | 264/3297 | 88/1098 | chr4 | 56382564 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338310
|
C | CTTCT | 3 | a0003c0003t0002a0008c0011t0002a0018c0023t0002 | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*88_*91dupAGAA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 91 | chr4 | 56338310 | |||||
chr4:56338329
|
G | A | 1 | a0005c0007t0003 | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*73C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 73 | chr4 | 56338329 | |||||
chr4:56338336
|
T | C | 1 | a0002c0002t0007 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 66 | chr4 | 56338336 | |||||
chr4:56387405
|
C | T | 1 | a0004c0004t0006 | 1 | NA18946.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/15 | 3106 | chr4 | 56387405 | |||||
chr4:56387411
|
T | C | 1 | a0006c0009t0004 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-92A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/15 | chr4 | 56387411 | ||||||
chr4:56387451
|
C | T | 1 | a0001c0005t0005 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/15 | 3152 | chr4 | 56387451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338794
|
A | G | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.2908-3T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56338794 | ||||||
chr4:56338892
|
G | A | 2 | a0003c0003t0002g0046a0003c0003t0002g0049 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2908-101C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56338892 | ||||||
chr4:56339033
|
G | A | 1 | a0002c0002t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2908-242C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339033 | ||||||
chr4:56339093
|
C | G | 2 | a0005c0007t0003g0035a0005c0007t0003g0037 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2908-302G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339093 | ||||||
chr4:56339162
|
A | AT | 87 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(84): Show | 98 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(95): Show |
intron_variant | MODIFIER | c.2908-372dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339162 | ||||||
chr4:56339165
|
T | A | 2 | a0003c0003t0002g0277a0003c0003t0002g0279 | 2 | HG00738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2908-374A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339165 | ||||||
chr4:56339191
|
T | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.2908-400A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339191 | ||||||
chr4:56339204
|
A | C | 26 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(23): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2908-413T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339204 | ||||||
chr4:56339210
|
G | C | 3 | a0003c0003t0002g0046a0003c0003t0002g0049a0003c0003t0002g0052 | 3 | HG02896.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2908-419C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339210 | ||||||
chr4:56339292
|
C | T | 1 | a0002c0002t0001g0202 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2908-501G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339292 | ||||||
chr4:56339293
|
G | A | 2 | a0003c0003t0002g0248a0003c0003t0002g0249 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2908-502C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339293 | ||||||
chr4:56339344
|
A | G | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2908-553T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339344 | ||||||
chr4:56339387
|
C | T | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.2908-596G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339387 | ||||||
chr4:56339396
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2908-605G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339396 | ||||||
chr4:56339461
|
A | G | 1 | a0002c0002t0001g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2908-670T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339461 | ||||||
chr4:56339477
|
G | A | 1 | a0004c0004t0001g0135 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2908-686C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339477 | ||||||
chr4:56339622
|
A | G | 264 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(261): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.2908-831T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339622 | ||||||
chr4:56339668
|
T | C | 172 | a0001c0001t0001g0166a0001c0005t0001g0011a0001c0005t0001g0028others(169): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2908-877A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339668 | ||||||
chr4:56339680
|
G | C | 2 | a0002c0002t0001g0190a0002c0002t0001g0198 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2908-889C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339680 | ||||||
chr4:56339703
|
A | T | 1 | a0009c0012t0001g0152 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2908-912T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339703 | ||||||
chr4:56339748
|
C | CA | 22 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(19): Show | 25 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2908-958dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | ||||||
chr4:56339748
|
C | CAA | 71 | a0001c0001t0001g0125a0002c0002t0001g0002a0002c0002t0001g0009others(68): Show | 81 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2908-959_2908-958d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | ||||||
chr4:56339748
|
C | CAAA | 131 | a0001c0001t0001g0166a0001c0005t0001g0242a0001c0005t0001g0299others(128): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.2908-960_2908-958d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | ||||||
chr4:56339748
|
C | CAAAA | 38 | a0001c0005t0001g0011a0001c0005t0001g0032a0001c0005t0001g0050others(35): Show | 40 | HG00323.hp1 HG00544.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.2908-961_2908-958d others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | ||||||
chr4:56339748
|
CA | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0073others(4): Show | 7 | HG00099.hp2 HG01515.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2908-958delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | ||||||
chr4:56339830
|
A | AAG | 171 | a0001c0001t0001g0166a0001c0005t0001g0011a0001c0005t0001g0028others(168): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2908-1041_2908-104 others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339830 | ||||||
chr4:56339891
|
A | G | 1 | a0003c0003t0002g0252 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2908-1100T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339891 | ||||||
chr4:56339908
|
C | T | 1 | a0004c0004t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2908-1117G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339908 | ||||||
chr4:56340028
|
G | T | 1 | a0002c0002t0001g0113 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2908-1237C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340028 | ||||||
chr4:56340077
|
G | GAGAA | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2908-1290_2908-128 others(8): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340077 | ||||||
chr4:56340087
|
T | C | 1 | a0002c0002t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2908-1296A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340087 | ||||||
chr4:56340133
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01109.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2908-1342G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340133 | ||||||
chr4:56340147
|
C | T | 1 | a0001c0005t0001g0314 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2908-1356G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340147 | ||||||
chr4:56340164
|
A | T | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2908-1373T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340164 | ||||||
chr4:56340226
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2908-1435G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340226 | ||||||
chr4:56340319
|
G | A | 1 | a0003c0003t0002g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2908-1528C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340319 | ||||||
chr4:56340379
|
G | A | 1 | a0001c0005t0001g0309 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2908-1588C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340379 | ||||||
chr4:56340410
|
T | C | 1 | a0008c0011t0002g0205 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2908-1619A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340410 | ||||||
chr4:56340430
|
C | G | 1 | a0002c0002t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2908-1639G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340430 | ||||||
chr4:56340474
|
C | T | 1 | a0004c0004t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2908-1683G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340474 | ||||||
chr4:56340608
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2908-1817G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340608 | ||||||
chr4:56340998
|
A | C | 5 | a0003c0003t0002g0010a0003c0003t0002g0257a0003c0003t0002g0260others(2): Show | 7 | HG00140.hp2 HG00280.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2907+1837T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340998 | ||||||
chr4:56341022
|
G | A | 208 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(205): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2907+1813C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341022 | ||||||
chr4:56341178
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1657T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341178 | ||||||
chr4:56341181
|
T | C | 2 | a0002c0002t0001g0177a0012c0015t0001g0194 | 2 | NA18997.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2907+1654A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341181 | ||||||
chr4:56341389
|
C | CT | 84 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0095others(81): Show | 96 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.2907+1445dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTT | 10 | a0002c0002t0001g0108a0002c0002t0001g0178a0002c0002t0001g0181others(7): Show | 10 | HG01074.hp1 HG01346.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.2907+1444_2907+144 others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTT | 8 | a0002c0002t0001g0180a0005c0007t0003g0033a0005c0007t0003g0034others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2907+1443_2907+144 others(7): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(2): Show |
28 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(25): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2907+1437_2907+144 others(13): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(3): Show |
26 | a0003c0003t0002g0027a0003c0003t0002g0044a0003c0003t0002g0047others(23): Show | 27 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2907+1436_2907+144 others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(4): Show |
8 | a0003c0003t0002g0045a0003c0003t0002g0046a0003c0003t0002g0049others(5): Show | 8 | HG01175.hp2 HG01258.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1435_2907+144 others(15): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(5): Show |
3 | a0003c0003t0002g0256a0003c0003t0002g0292a0011c0014t0001g0282 | 3 | HG03471.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2907+1434_2907+144 others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(6): Show |
2 | a0003c0003t0002g0290a0003c0003t0002g0291 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2907+1433_2907+144 others(17): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(7): Show |
3 | a0001c0010t0001g0280a0003c0003t0002g0240a0003c0003t0002g0241 | 3 | HG02895.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2907+1432_2907+144 others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
C | CTTTTTTT others(10): Show |
1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2907+1429_2907+144 others(21): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
CT | C | 52 | a0001c0001t0001g0125a0001c0001t0001g0166a0003c0003t0002g0263others(49): Show | 60 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2907+1445delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341389
|
CTTTTTT | C | 35 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(32): Show | 38 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2907+1440_2907+144 others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | ||||||
chr4:56341424
|
C | T | 1 | a0004c0004t0001g0151 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2907+1411G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341424 | ||||||
chr4:56341446
|
G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1389C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341446 | ||||||
chr4:56341559
|
A | AT | 128 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0071others(125): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2907+1275dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341559 | ||||||
chr4:56341559
|
AT | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1275delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341559 | ||||||
chr4:56341591
|
C | T | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2907+1244G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341591 | ||||||
chr4:56341676
|
C | T | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2907+1159G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341676 | ||||||
chr4:56341840
|
G | A | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2907+995C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341840 | ||||||
chr4:56341941
|
G | A | 53 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(50): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.2907+894C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341941 | ||||||
chr4:56342004
|
C | T | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2907+831G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342004 | ||||||
chr4:56342038
|
T | C | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2907+797A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342038 | ||||||
chr4:56342043
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+792G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342043 | ||||||
chr4:56342063
|
G | C | 3 | a0004c0004t0001g0136a0004c0004t0001g0151a0004c0004t0001g0156 | 3 | NA18612.hp2 NA18961.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2907+772C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342063 | ||||||
chr4:56342110
|
C | CA | 56 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0125others(53): Show | 65 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2907+724dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342110 | ||||||
chr4:56342110
|
CA | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0090a0001c0001t0001g0099others(12): Show | 16 | HG00408.hp1 HG01346.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.2907+724delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342110 | ||||||
chr4:56342110
|
CAAAAAAA others(9): Show |
C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2907+709_2907+724d others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342110 | ||||||
chr4:56342111
|
A | C | 1 | a0013c0017t0001g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2907+724T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342111 | ||||||
chr4:56342165
|
TAA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+668_2907+669d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342165 | ||||||
chr4:56342284
|
A | G | 1 | a0003c0003t0002g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2907+551T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342284 | ||||||
chr4:56342393
|
A | G | 1 | a0002c0002t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2907+442T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342393 | ||||||
chr4:56342594
|
T | C | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.2907+241A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342594 | ||||||
chr4:56342604
|
T | C | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2907+231A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342604 | ||||||
chr4:56342651
|
C | T | 1 | a0003c0003t0002g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2907+184G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342651 | ||||||
chr4:56342789
|
A | T | 150 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(147): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2907+46T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342789 | ||||||
chr4:56343295
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0073others(2): Show | 6 | HG01081.hp1 HG01192.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.2775+267G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343295 | ||||||
chr4:56343340
|
AAAC | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.2775+219_2775+221d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343340 | ||||||
chr4:56343359
|
A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+203T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343359 | ||||||
chr4:56343363
|
T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+199A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343363 | ||||||
chr4:56343365
|
C | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+197G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343365 | ||||||
chr4:56343365
|
CAT | C | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2775+195_2775+196d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343365 | ||||||
chr4:56343365
|
CATAT | C | 227 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(224): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2775+193_2775+196d others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343365 | ||||||
chr4:56343369
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+193A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343369 | ||||||
chr4:56343480
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2775+82G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343480 | ||||||
chr4:56343873
|
A | C | 2 | a0001c0005t0001g0303a0001c0005t0001g0321 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2653-189T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56343873 | ||||||
chr4:56344034
|
G | A | 2 | a0002c0002t0001g0119a0002c0002t0001g0121 | 2 | NA18975.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2653-350C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344034 | ||||||
chr4:56344056
|
A | C | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2653-372T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344056 | ||||||
chr4:56344159
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653-475A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344159 | ||||||
chr4:56344164
|
A | T | 1 | a0003c0003t0002g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2653-480T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344164 | ||||||
chr4:56344170
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653-486C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344170 | ||||||
chr4:56344257
|
C | T | 1 | a0004c0004t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2653-573G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344257 | ||||||
chr4:56344343
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653-659G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344343 | ||||||
chr4:56344344
|
A | C | 2 | a0001c0005t0001g0307a0001c0005t0001g0322 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2653-660T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344344 | ||||||
chr4:56344348
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2653-664A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344348 | ||||||
chr4:56344600
|
C | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2652+527G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344600 | ||||||
chr4:56344740
|
T | C | 1 | a0004c0004t0001g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2652+387A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344740 | ||||||
chr4:56344940
|
C | CT | 9 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0283others(6): Show | 10 | HG00438.hp2 HG01261.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2652+186dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344940 | ||||||
chr4:56344940
|
CT | C | 116 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0005t0001g0011others(113): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2652+186delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344940 | ||||||
chr4:56344944
|
T | C | 79 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(76): Show | 90 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.2652+183A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344944 | ||||||
chr4:56344945
|
T | C | 4 | a0002c0002t0001g0185a0002c0002t0001g0198a0002c0002t0001g0217others(1): Show | 4 | HG01943.hp1 NA18953.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2652+182A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344945 | ||||||
chr4:56344948
|
T | C | 1 | a0002c0002t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2652+179A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344948 | ||||||
chr4:56345090
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2652+37G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56345090 | ||||||
chr4:56345366
|
A | G | 59 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0023others(56): Show | 67 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.2489-76T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345366 | ||||||
chr4:56345623
|
C | T | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2489-333G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345623 | ||||||
chr4:56345676
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-386T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345676 | ||||||
chr4:56345705
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0104 | 2 | NA18941.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2489-415T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345705 | ||||||
chr4:56345884
|
C | G | 3 | a0003c0003t0002g0263a0003c0003t0002g0275a0003c0003t0002g0289 | 3 | HG02055.hp1 HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2489-594G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345884 | ||||||
chr4:56345935
|
G | A | 1 | a0003c0003t0002g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2489-645C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345935 | ||||||
chr4:56346044
|
G | A | 3 | a0001c0005t0001g0285a0001c0005t0001g0299a0001c0005t0001g0300 | 3 | NA18944.hp2 NA19011.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2489-754C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346044 | ||||||
chr4:56346098
|
T | C | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2489-808A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346098 | ||||||
chr4:56346148
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0164 | 2 | NA18940.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2489-858A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346148 | ||||||
chr4:56346243
|
G | A | 3 | a0004c0004t0001g0130a0004c0004t0001g0137a0004c0004t0001g0148 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2489-953C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346243 | ||||||
chr4:56346437
|
A | G | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-1147T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346437 | ||||||
chr4:56346569
|
G | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2489-1279C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346569 | ||||||
chr4:56346613
|
A | C | 2 | a0003c0003t0002g0269a0003c0003t0002g0276 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2489-1323T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346613 | ||||||
chr4:56346620
|
A | G | 2 | a0003c0003t0002g0269a0003c0003t0002g0276 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2489-1330T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346620 | ||||||
chr4:56346849
|
C | T | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2489-1559G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346849 | ||||||
chr4:56346879
|
C | CAAAAATT others(329): Show |
1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2489-1590_2489-158 others(340): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346879 | ||||||
chr4:56346997
|
C | T | 1 | a0002c0002t0001g0009 | 3 | HG01243.hp2 HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2489-1707G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346997 | ||||||
chr4:56347026
|
G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489-1736C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347026 | ||||||
chr4:56347040
|
T | TA | 18 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0010t0001g0280others(15): Show | 18 | HG00423.hp2 HG01175.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2489-1751dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347040 | ||||||
chr4:56347041
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100 | 4 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489-1751T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347041 | ||||||
chr4:56347124
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2489-1834A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347124 | ||||||
chr4:56347137
|
A | G | 1 | a0002c0002t0001g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2489-1847T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347137 | ||||||
chr4:56347692
|
G | A | 203 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(200): Show | 224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2488+1571C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347692 | ||||||
chr4:56347705
|
C | A | 1 | a0011c0014t0001g0282 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2488+1558G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347705 | ||||||
chr4:56347776
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2488+1487G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347776 | ||||||
chr4:56347891
|
A | C | 1 | a0003c0003t0002g0293 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2488+1372T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347891 | ||||||
chr4:56347903
|
A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+1360T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347903 | ||||||
chr4:56347958
|
C | G | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2488+1305G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347958 | ||||||
chr4:56348200
|
T | G | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.2488+1063A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348200 | ||||||
chr4:56348241
|
C | T | 212 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(209): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2488+1022G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348241 | ||||||
chr4:56348258
|
C | CT | 14 | a0002c0002t0001g0226a0002c0002t0001g0235a0003c0003t0001g0220others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2488+1004dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348258 | ||||||
chr4:56348422
|
T | G | 1 | a0004c0004t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2488+841A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348422 | ||||||
chr4:56348506
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+757A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348506 | ||||||
chr4:56348606
|
C | T | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2488+657G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348606 | ||||||
chr4:56348691
|
T | C | 1 | a0002c0002t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2488+572A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348691 | ||||||
chr4:56348832
|
C | T | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2488+431G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348832 | ||||||
chr4:56348933
|
G | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+330C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348933 | ||||||
chr4:56349221
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+42A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56349221 | ||||||
chr4:56350102
|
A | G | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1693-44T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350102 | ||||||
chr4:56350174
|
G | T | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1693-116C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350174 | ||||||
chr4:56350176
|
C | T | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1693-118G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350176 | ||||||
chr4:56350177
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1693-119C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350177 | ||||||
chr4:56350364
|
G | T | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0018c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693-306C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350364 | ||||||
chr4:56350373
|
G | A | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1693-315C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350373 | ||||||
chr4:56350411
|
G | A | 2 | a0004c0004t0001g0139a0004c0004t0001g0221 | 2 | HG00438.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1693-353C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350411 | ||||||
chr4:56350426
|
C | T | 3 | a0003c0003t0002g0255a0003c0003t0002g0270a0003c0003t0002g0288 | 3 | HG00140.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1693-368G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350426 | ||||||
chr4:56350456
|
A | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693-398T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350456 | ||||||
chr4:56350622
|
T | C | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | NA18949.hp2 NA18954.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693-564A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350622 | ||||||
chr4:56350690
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1693-632A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350690 | ||||||
chr4:56350731
|
T | C | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1692+611A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350731 | ||||||
chr4:56350766
|
G | A | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1692+576C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350766 | ||||||
chr4:56350773
|
A | G | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1692+569T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350773 | ||||||
chr4:56350775
|
G | A | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1692+567C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350775 | ||||||
chr4:56350785
|
T | A | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1692+557A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350785 | ||||||
chr4:56350884
|
T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.1692+458A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350884 | ||||||
chr4:56350915
|
T | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1692+427A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350915 | ||||||
chr4:56351057
|
G | A | 9 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692+285C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351057 | ||||||
chr4:56351130
|
T | C | 1 | a0003c0003t0002g0295 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1692+212A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351130 | ||||||
chr4:56351174
|
T | C | 122 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(119): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1692+168A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351174 | ||||||
chr4:56351194
|
A | G | 1 | a0004c0004t0001g0142 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1692+148T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351194 | ||||||
chr4:56351506
|
C | T | 1 | a0002c0002t0001g0202 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1577-49G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351506 | ||||||
chr4:56351538
|
T | C | 1 | a0015c0021t0001g0325 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1577-81A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351538 | ||||||
chr4:56351629
|
C | G | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1577-172G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351629 | ||||||
chr4:56351754
|
A | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.1577-297T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351754 | ||||||
chr4:56351917
|
C | CA | 9 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 10 | HG01258.hp2 HG01433.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1577-461dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351917 | ||||||
chr4:56351917
|
CA | C | 139 | a0001c0001t0001g0073a0001c0005t0001g0011a0001c0005t0001g0028others(136): Show | 154 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1577-461delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351917 | ||||||
chr4:56352228
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1577-771G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352228 | ||||||
chr4:56352230
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1577-773G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352230 | ||||||
chr4:56352277
|
T | A | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.1577-820A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352277 | ||||||
chr4:56352497
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01109.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1576+907C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352497 | ||||||
chr4:56352538
|
C | T | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1576+866G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352538 | ||||||
chr4:56352559
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1576+845T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352559 | ||||||
chr4:56352606
|
G | A | 1 | a0001c0005t0005g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1576+798C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352606 | ||||||
chr4:56352843
|
G | A | 1 | a0001c0005t0001g0285 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1576+561C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352843 | ||||||
chr4:56352971
|
C | T | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1576+433G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352971 | ||||||
chr4:56353009
|
CT | C | 10 | a0001c0001t0001g0065a0001c0005t0001g0318a0005c0007t0003g0033others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1576+394delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353009 | ||||||
chr4:56353019
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1576+385A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353019 | ||||||
chr4:56353094
|
C | T | 2 | a0003c0003t0002g0269a0003c0003t0002g0276 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1576+310G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353094 | ||||||
chr4:56353209
|
T | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1576+195A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353209 | ||||||
chr4:56353250
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576+154T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353250 | ||||||
chr4:56353263
|
G | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576+141C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353263 | ||||||
chr4:56353328
|
A | T | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1576+76T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353328 | ||||||
chr4:56353357
|
A | G | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1576+47T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353357 | ||||||
chr4:56353396
|
T | A | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | splice_region_variant&intron_variant | LOW | c.1576+8A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353396 | ||||||
chr4:56353892
|
C | T | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1383+147G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353892 | ||||||
chr4:56353954
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1383+85A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353954 | ||||||
chr4:56353957
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1383+82T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353957 | ||||||
chr4:56353962
|
C | A | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1383+77G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353962 | ||||||
chr4:56354631
|
C | T | 1 | a0002c0002t0001g0227 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1210+74G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 7/14 | chr4 | 56354631 | ||||||
chr4:56354827
|
A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104-16T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56354827 | ||||||
chr4:56354828
|
C | T | 2 | a0001c0005t0001g0303a0001c0005t0001g0321 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1104-17G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56354828 | ||||||
chr4:56354918
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104-107G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56354918 | ||||||
chr4:56355149
|
C | A | 1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1103+33G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56355149 | ||||||
chr4:56355448
|
A | G | 4 | a0007c0008t0001g0059a0007c0008t0001g0060a0007c0008t0001g0061others(1): Show | 4 | HG03041.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-25T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355448 | ||||||
chr4:56355561
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.862-138A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355561 | ||||||
chr4:56355593
|
G | GT | 51 | a0001c0001t0001g0015a0001c0001t0001g0079a0001c0001t0001g0080others(48): Show | 60 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.862-171dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355593 | ||||||
chr4:56355593
|
GT | G | 109 | a0001c0001t0001g0090a0001c0005t0001g0011a0001c0005t0001g0028others(106): Show | 120 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.862-171delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355593 | ||||||
chr4:56355593
|
GTT | G | 89 | a0001c0010t0001g0280a0001c0010t0001g0281a0002c0002t0001g0017others(86): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-172_862-171del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355593 | ||||||
chr4:56355594
|
T | TG | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-172_862-171ins others(1): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355594 | ||||||
chr4:56355596
|
T | G | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.862-173A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355596 | ||||||
chr4:56355641
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.862-218G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355641 | ||||||
chr4:56355749
|
G | A | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.862-326C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355749 | ||||||
chr4:56355792
|
A | T | 209 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(206): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.862-369T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355792 | ||||||
chr4:56355882
|
T | A | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.862-459A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355882 | ||||||
chr4:56355932
|
A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-509T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355932 | ||||||
chr4:56356127
|
C | T | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.862-704G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356127 | ||||||
chr4:56356211
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.862-788A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356211 | ||||||
chr4:56356260
|
A | G | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.862-837T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356260 | ||||||
chr4:56356332
|
A | C | 1 | a0003c0003t0002g0264 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.862-909T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356332 | ||||||
chr4:56356345
|
T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-922A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356345 | ||||||
chr4:56356368
|
C | A | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-945G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356368 | ||||||
chr4:56356463
|
A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-1040T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356463 | ||||||
chr4:56356498
|
T | C | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.862-1075A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356498 | ||||||
chr4:56356615
|
C | A | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.862-1192G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356615 | ||||||
chr4:56356820
|
C | T | 1 | a0003c0003t0002g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.862-1397G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356820 | ||||||
chr4:56356875
|
C | T | 1 | a0004c0004t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.862-1452G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356875 | ||||||
chr4:56356901
|
C | T | 1 | a0002c0002t0001g0110 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.862-1478G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356901 | ||||||
chr4:56357084
|
A | G | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.862-1661T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357084 | ||||||
chr4:56357155
|
T | A | 53 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(50): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.862-1732A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357155 | ||||||
chr4:56357186
|
T | C | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.862-1763A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357186 | ||||||
chr4:56357516
|
C | T | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.862-2093G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357516 | ||||||
chr4:56357519
|
C | A | 4 | a0004c0004t0001g0020a0004c0004t0001g0127a0004c0004t0001g0131others(1): Show | 5 | NA18977.hp1 NA18994.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-2096G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357519 | ||||||
chr4:56357520
|
C | G | 4 | a0004c0004t0001g0020a0004c0004t0001g0127a0004c0004t0001g0131others(1): Show | 5 | NA18977.hp1 NA18994.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-2097G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357520 | ||||||
chr4:56357639
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.862-2216A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357639 | ||||||
chr4:56357704
|
A | C | 1 | a0003c0003t0002g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.862-2281T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357704 | ||||||
chr4:56358173
|
T | C | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.862-2750A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358173 | ||||||
chr4:56358185
|
T | A | 1 | a0001c0010t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.862-2762A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358185 | ||||||
chr4:56358316
|
C | A | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.862-2893G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358316 | ||||||
chr4:56358353
|
A | G | 122 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(119): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.862-2930T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358353 | ||||||
chr4:56358462
|
C | T | 7 | a0001c0005t0001g0285a0001c0005t0001g0299a0001c0005t0001g0300others(4): Show | 7 | HG02056.hp1 NA18944.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.862-3039G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358462 | ||||||
chr4:56358463
|
G | A | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.862-3040C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358463 | ||||||
chr4:56358838
|
T | A | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0018c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.862-3415A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358838 | ||||||
chr4:56358883
|
A | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.862-3460T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358883 | ||||||
chr4:56359003
|
A | G | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-3580T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359003 | ||||||
chr4:56359007
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-3584G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359007 | ||||||
chr4:56359112
|
G | GT | 124 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(121): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.862-3690dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359112 | ||||||
chr4:56359299
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.862-3876G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359299 | ||||||
chr4:56359317
|
C | A | 1 | a0002c0002t0001g0213 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.862-3894G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359317 | ||||||
chr4:56359324
|
C | CGCCTCCT | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-3908_862-3902d others(9): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359324 | ||||||
chr4:56359338
|
T | C | 1 | a0003c0003t0002g0257 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.862-3915A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359338 | ||||||
chr4:56359345
|
C | T | 1 | a0002c0002t0001g0227 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.862-3922G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359345 | ||||||
chr4:56359346
|
G | A | 1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.862-3923C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359346 | ||||||
chr4:56359369
|
C | G | 1 | a0003c0003t0002g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.862-3946G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359369 | ||||||
chr4:56359507
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4084C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359507 | ||||||
chr4:56359535
|
G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4112C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359535 | ||||||
chr4:56359550
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.862-4127C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359550 | ||||||
chr4:56359617
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.862-4194C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359617 | ||||||
chr4:56359622
|
A | G | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.862-4199T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359622 | ||||||
chr4:56359645
|
A | AC | 8 | a0001c0001t0001g0078a0001c0001t0001g0162a0001c0005t0001g0050others(5): Show | 8 | HG01243.hp1 HG02040.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4223dupG | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359645 | ||||||
chr4:56359662
|
G | A | 1 | a0002c0002t0001g0019 | 2 | NA18951.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.862-4239C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359662 | ||||||
chr4:56359701
|
G | A | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.862-4278C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359701 | ||||||
chr4:56359748
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4325T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359748 | ||||||
chr4:56359908
|
A | G | 1 | a0001c0005t0001g0306 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.862-4485T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359908 | ||||||
chr4:56360234
|
G | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-4811C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360234 | ||||||
chr4:56360255
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.862-4832T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360255 | ||||||
chr4:56360284
|
T | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.862-4861A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360284 | ||||||
chr4:56360338
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4915C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360338 | ||||||
chr4:56360471
|
A | G | 1 | a0011c0014t0001g0282 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.862-5048T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360471 | ||||||
chr4:56360689
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.862-5266C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360689 | ||||||
chr4:56360692
|
C | T | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.862-5269G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360692 | ||||||
chr4:56360728
|
A | G | 10 | a0003c0003t0002g0027a0003c0003t0002g0239a0003c0003t0002g0266others(7): Show | 11 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.862-5305T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360728 | ||||||
chr4:56360753
|
C | T | 5 | a0007c0008t0001g0059a0007c0008t0001g0060a0007c0008t0001g0061others(2): Show | 5 | HG02145.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.862-5330G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360753 | ||||||
chr4:56360793
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0161 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.862-5370A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360793 | ||||||
chr4:56360857
|
C | T | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-5434G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360857 | ||||||
chr4:56360886
|
A | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-5463T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360886 | ||||||
chr4:56360931
|
C | T | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-5508G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360931 | ||||||
chr4:56361133
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.862-5710G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361133 | ||||||
chr4:56361182
|
C | T | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.862-5759G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361182 | ||||||
chr4:56361183
|
G | A | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.862-5760C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361183 | ||||||
chr4:56361209
|
C | T | 51 | a0002c0002t0001g0002a0002c0002t0001g0023a0002c0002t0001g0177others(48): Show | 57 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.862-5786G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361209 | ||||||
chr4:56361242
|
C | G | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.862-5819G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361242 | ||||||
chr4:56361339
|
G | A | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-5916C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361339 | ||||||
chr4:56361504
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-6081G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361504 | ||||||
chr4:56361555
|
T | C | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.862-6132A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361555 | ||||||
chr4:56361686
|
T | C | 1 | a0001c0005t0001g0305 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.862-6263A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361686 | ||||||
chr4:56361774
|
C | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-6351G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361774 | ||||||
chr4:56361812
|
G | T | 2 | a0002c0002t0001g0112a0002c0002t0001g0116 | 2 | NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.862-6389C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361812 | ||||||
chr4:56362019
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-6596C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362019 | ||||||
chr4:56362263
|
C | G | 87 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(84): Show | 98 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(95): Show |
intron_variant | MODIFIER | c.862-6840G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362263 | ||||||
chr4:56362334
|
G | T | 5 | a0001c0005t0001g0301a0001c0005t0001g0303a0001c0005t0001g0304others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.862-6911C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362334 | ||||||
chr4:56362598
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.862-7175T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362598 | ||||||
chr4:56362748
|
C | G | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-7325G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362748 | ||||||
chr4:56362805
|
G | A | 53 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(50): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.862-7382C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362805 | ||||||
chr4:56362823
|
G | A | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.862-7400C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362823 | ||||||
chr4:56362878
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0199 | 3 | NA18973.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.862-7455C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362878 | ||||||
chr4:56362898
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.862-7475G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362898 | ||||||
chr4:56363009
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-7586G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363009 | ||||||
chr4:56363044
|
T | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.862-7621A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363044 | ||||||
chr4:56363058
|
G | A | 1 | a0003c0003t0002g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.862-7635C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363058 | ||||||
chr4:56363109
|
C | T | 1 | a0002c0002t0001g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.862-7686G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363109 | ||||||
chr4:56363110
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-7687C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363110 | ||||||
chr4:56363151
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-7728G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363151 | ||||||
chr4:56363185
|
C | A | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.862-7762G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363185 | ||||||
chr4:56363192
|
G | A | 1 | a0003c0003t0002g0297 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.862-7769C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363192 | ||||||
chr4:56363195
|
G | A | 1 | a0003c0003t0002g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.862-7772C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363195 | ||||||
chr4:56363195
|
G | C | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-7772C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363195 | ||||||
chr4:56363242
|
G | A | 10 | a0004c0004t0001g0020a0004c0004t0001g0127a0004c0004t0001g0128others(7): Show | 11 | NA18955.hp1 NA18960.hp2 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.862-7819C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363242 | ||||||
chr4:56363242
|
G | C | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.862-7819C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363242 | ||||||
chr4:56363293
|
G | T | 1 | a0002c0002t0001g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.862-7870C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363293 | ||||||
chr4:56363419
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-7996A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363419 | ||||||
chr4:56363447
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+8004C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363447 | ||||||
chr4:56363490
|
A | G | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+7961T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363490 | ||||||
chr4:56363499
|
G | A | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+7952C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363499 | ||||||
chr4:56363713
|
C | T | 1 | a0003c0003t0002g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.861+7738G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363713 | ||||||
chr4:56363791
|
G | C | 122 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(119): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.861+7660C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363791 | ||||||
chr4:56363792
|
G | A | 1 | a0002c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.861+7659C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363792 | ||||||
chr4:56363853
|
T | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+7598A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363853 | ||||||
chr4:56363854
|
G | A | 16 | a0003c0003t0002g0027a0003c0003t0002g0239a0003c0003t0002g0243others(13): Show | 17 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.861+7597C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363854 | ||||||
chr4:56363925
|
A | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+7526T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363925 | ||||||
chr4:56363991
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+7460C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363991 | ||||||
chr4:56364010
|
T | C | 115 | a0001c0001t0001g0088a0001c0005t0001g0011a0001c0005t0001g0028others(112): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.861+7441A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364010 | ||||||
chr4:56364052
|
C | T | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.861+7399G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364052 | ||||||
chr4:56364091
|
T | C | 1 | a0002c0002t0001g0120 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.861+7360A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364091 | ||||||
chr4:56364242
|
T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+7209A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364242 | ||||||
chr4:56364291
|
T | A | 1 | a0003c0003t0002g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.861+7160A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364291 | ||||||
chr4:56364307
|
A | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+7144T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364307 | ||||||
chr4:56364384
|
T | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+7067A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364384 | ||||||
chr4:56364427
|
G | A | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+7024C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364427 | ||||||
chr4:56364521
|
C | T | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+6930G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364521 | ||||||
chr4:56364709
|
T | C | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.861+6742A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364709 | ||||||
chr4:56364718
|
T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6733A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364718 | ||||||
chr4:56364765
|
T | C | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.861+6686A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364765 | ||||||
chr4:56364850
|
T | A | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.861+6601A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364850 | ||||||
chr4:56364883
|
G | T | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.861+6568C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364883 | ||||||
chr4:56364920
|
T | G | 1 | a0002c0002t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.861+6531A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364920 | ||||||
chr4:56364972
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6479A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364972 | ||||||
chr4:56365076
|
C | T | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.861+6375G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365076 | ||||||
chr4:56365095
|
A | T | 1 | a0004c0004t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.861+6356T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365095 | ||||||
chr4:56365117
|
AAAGAAGG others(728): Show |
A | 1 | a0007c0008t0001g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.861+5599_861+6333d others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365117 | ||||||
chr4:56365198
|
G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6253C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365198 | ||||||
chr4:56365226
|
T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6225A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365226 | ||||||
chr4:56365271
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+6180C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365271 | ||||||
chr4:56365276
|
T | C | 6 | a0001c0010t0001g0280a0001c0010t0001g0281a0007c0008t0001g0059others(3): Show | 6 | HG02809.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+6175A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365276 | ||||||
chr4:56365300
|
G | C | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+6151C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365300 | ||||||
chr4:56365309
|
C | A | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.861+6142G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365309 | ||||||
chr4:56365365
|
G | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0074others(10): Show | 16 | HG00597.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.861+6086C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365365 | ||||||
chr4:56365373
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0161 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.861+6078G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365373 | ||||||
chr4:56365409
|
A | C | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+6042T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365409 | ||||||
chr4:56365458
|
A | C | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.861+5993T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365458 | ||||||
chr4:56365576
|
C | T | 44 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.861+5875G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365576 | ||||||
chr4:56365604
|
T | C | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.861+5847A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365604 | ||||||
chr4:56365606
|
C | A | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+5845G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365606 | ||||||
chr4:56365614
|
T | A | 1 | a0004c0004t0001g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.861+5837A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365614 | ||||||
chr4:56365650
|
C | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+5801G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365650 | ||||||
chr4:56365671
|
C | T | 1 | a0018c0023t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.861+5780G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365671 | ||||||
chr4:56365696
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.861+5755T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365696 | ||||||
chr4:56365708
|
G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+5743C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365708 | ||||||
chr4:56365732
|
A | C | 4 | a0003c0003t0002g0262a0003c0003t0002g0290a0003c0003t0002g0291others(1): Show | 4 | HG02055.hp2 HG02622.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.861+5719T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365732 | ||||||
chr4:56365757
|
A | G | 44 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.861+5694T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365757 | ||||||
chr4:56365825
|
C | G | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+5626G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365825 | ||||||
chr4:56365866
|
G | A | 1 | a0007c0008t0001g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.861+5585C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365866 | ||||||
chr4:56365940
|
T | C | 3 | a0003c0003t0002g0255a0003c0003t0002g0270a0003c0003t0002g0288 | 3 | HG00140.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.861+5511A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365940 | ||||||
chr4:56365950
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+5501G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365950 | ||||||
chr4:56365967
|
T | C | 1 | a0002c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.861+5484A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365967 | ||||||
chr4:56366011
|
G | A | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.861+5440C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366011 | ||||||
chr4:56366013
|
T | C | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861+5438A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366013 | ||||||
chr4:56366128
|
G | A | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.861+5323C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366128 | ||||||
chr4:56366236
|
C | T | 4 | a0001c0001t0001g0013a0003c0003t0002g0003a0003c0003t0002g0042others(1): Show | 8 | HG00408.hp2 HG01167.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+5215G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366236 | ||||||
chr4:56366237
|
G | C | 53 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(50): Show | 56 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.861+5214C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366237 | ||||||
chr4:56366257
|
C | G | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.861+5194G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366257 | ||||||
chr4:56366274
|
C | T | 2 | a0002c0002t0001g0178a0002c0002t0001g0179 | 2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.861+5177G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366274 | ||||||
chr4:56366301
|
G | A | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.861+5150C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366301 | ||||||
chr4:56366398
|
C | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+5053G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366398 | ||||||
chr4:56366541
|
C | G | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.861+4910G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366541 | ||||||
chr4:56366570
|
G | A | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+4881C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366570 | ||||||
chr4:56366723
|
A | G | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.861+4728T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366723 | ||||||
chr4:56366804
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.861+4647G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366804 | ||||||
chr4:56366808
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+4643G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366808 | ||||||
chr4:56366837
|
T | G | 53 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(50): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.861+4614A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366837 | ||||||
chr4:56366867
|
C | T | 1 | a0002c0002t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.861+4584G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366867 | ||||||
chr4:56367040
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+4411T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367040 | ||||||
chr4:56367118
|
T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.861+4333A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367118 | ||||||
chr4:56367164
|
C | T | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.861+4287G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367164 | ||||||
chr4:56367170
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+4281C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367170 | ||||||
chr4:56367259
|
G | C | 4 | a0002c0002t0001g0002a0002c0002t0001g0196a0002c0002t0001g0197others(1): Show | 8 | HG00735.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+4192C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367259 | ||||||
chr4:56367272
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+4179G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367272 | ||||||
chr4:56367277
|
C | A | 2 | a0001c0005t0001g0311a0001c0005t0001g0317 | 2 | NA18989.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.861+4174G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367277 | ||||||
chr4:56367404
|
T | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+4047A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367404 | ||||||
chr4:56367436
|
C | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0199 | 3 | NA18973.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.861+4015G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367436 | ||||||
chr4:56367448
|
T | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+4003A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367448 | ||||||
chr4:56367453
|
C | A | 1 | a0002c0002t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.861+3998G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367453 | ||||||
chr4:56367466
|
T | C | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+3985A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367466 | ||||||
chr4:56367470
|
T | C | 212 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(209): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.861+3981A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367470 | ||||||
chr4:56367471
|
G | T | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.861+3980C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367471 | ||||||
chr4:56367597
|
G | C | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.861+3854C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367597 | ||||||
chr4:56367621
|
G | T | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.861+3830C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367621 | ||||||
chr4:56367639
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.861+3812A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367639 | ||||||
chr4:56367651
|
G | A | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.861+3800C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367651 | ||||||
chr4:56367692
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0161 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.861+3759G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367692 | ||||||
chr4:56367875
|
C | A | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+3576G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367875 | ||||||
chr4:56367896
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+3555G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367896 | ||||||
chr4:56367918
|
A | G | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+3533T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367918 | ||||||
chr4:56367971
|
T | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+3480A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367971 | ||||||
chr4:56367972
|
G | A | 1 | a0003c0003t0002g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.861+3479C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367972 | ||||||
chr4:56368028
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.861+3423T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368028 | ||||||
chr4:56368061
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+3390A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368061 | ||||||
chr4:56368103
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+3348T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368103 | ||||||
chr4:56368105
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+3346T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368105 | ||||||
chr4:56368150
|
A | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+3301T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368150 | ||||||
chr4:56368175
|
T | A | 1 | a0006c0009t0004g0029 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.861+3276A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368175 | ||||||
chr4:56368228
|
G | A | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.861+3223C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368228 | ||||||
chr4:56368264
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+3187C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368264 | ||||||
chr4:56368334
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.861+3117T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368334 | ||||||
chr4:56368395
|
T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.861+3056A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368395 | ||||||
chr4:56368432
|
C | T | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.861+3019G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368432 | ||||||
chr4:56368463
|
G | T | 1 | a0003c0003t0002g0239 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.861+2988C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368463 | ||||||
chr4:56368636
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+2815C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368636 | ||||||
chr4:56368651
|
T | C | 2 | a0002c0006t0001g0231a0002c0006t0001g0237 | 2 | NA18982.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.861+2800A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368651 | ||||||
chr4:56368709
|
G | C | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.861+2742C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368709 | ||||||
chr4:56368733
|
G | C | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+2718C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368733 | ||||||
chr4:56368808
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2643C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368808 | ||||||
chr4:56368868
|
T | TA | 9 | a0001c0001t0001g0091a0002c0002t0001g0198a0003c0003t0002g0044others(6): Show | 9 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.861+2582dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368868 | ||||||
chr4:56368878
|
AAC | A | 9 | a0003c0003t0002g0025a0003c0003t0002g0026a0003c0003t0002g0251others(6): Show | 11 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.861+2571_861+2572d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368878 | ||||||
chr4:56368879
|
AC | A | 44 | a0003c0003t0002g0010a0003c0003t0002g0027a0003c0003t0002g0238others(41): Show | 47 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.861+2571delG | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368879 | ||||||
chr4:56368897
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2554A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368897 | ||||||
chr4:56368904
|
CA | C | 8 | a0001c0001t0001g0071a0003c0003t0002g0044a0003c0003t0002g0045others(5): Show | 8 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2546delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368904 | ||||||
chr4:56368932
|
C | T | 1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.861+2519G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368932 | ||||||
chr4:56368978
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2473G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368978 | ||||||
chr4:56369120
|
T | C | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+2331A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369120 | ||||||
chr4:56369308
|
G | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+2143C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369308 | ||||||
chr4:56369341
|
C | G | 1 | a0001c0005t0001g0284 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.861+2110G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369341 | ||||||
chr4:56369585
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0159others(1): Show | 6 | NA18971.hp1 NA18975.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1866G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369585 | ||||||
chr4:56369593
|
G | A | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.861+1858C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369593 | ||||||
chr4:56369697
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.861+1754G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369697 | ||||||
chr4:56369746
|
C | G | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1705G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369746 | ||||||
chr4:56369837
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+1614C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369837 | ||||||
chr4:56369875
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.861+1576G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369875 | ||||||
chr4:56369944
|
T | TAA | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1505_861+1506d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369944 | ||||||
chr4:56369944
|
TA | T | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.861+1506delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369944 | ||||||
chr4:56369957
|
A | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.861+1494T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369957 | ||||||
chr4:56369958
|
A | C | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.861+1493T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369958 | ||||||
chr4:56370096
|
T | C | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.861+1355A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370096 | ||||||
chr4:56370160
|
T | A | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.861+1291A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370160 | ||||||
chr4:56370165
|
C | T | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.861+1286G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370165 | ||||||
chr4:56370181
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+1270C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370181 | ||||||
chr4:56370280
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+1171G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370280 | ||||||
chr4:56370287
|
C | T | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+1164G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370287 | ||||||
chr4:56370312
|
C | T | 1 | a0002c0002t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.861+1139G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370312 | ||||||
chr4:56370388
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.861+1063C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370388 | ||||||
chr4:56370416
|
G | GA | 5 | a0001c0005t0001g0032a0004c0004t0001g0142a0004c0004t0001g0143others(2): Show | 5 | HG04199.hp1 NA18969.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.861+1034dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370416 | ||||||
chr4:56370531
|
G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+920C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370531 | ||||||
chr4:56370563
|
C | T | 1 | a0003c0003t0002g0272 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.861+888G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370563 | ||||||
chr4:56370567
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+884T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370567 | ||||||
chr4:56370620
|
A | G | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861+831T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370620 | ||||||
chr4:56370657
|
A | G | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.861+794T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370657 | ||||||
chr4:56370775
|
A | C | 4 | a0007c0008t0001g0059a0007c0008t0001g0060a0007c0008t0001g0061others(1): Show | 4 | HG03041.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.861+676T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370775 | ||||||
chr4:56370824
|
T | C | 1 | a0002c0002t0001g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.861+627A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370824 | ||||||
chr4:56370994
|
T | G | 96 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(93): Show | 108 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(105): Show |
intron_variant | MODIFIER | c.861+457A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370994 | ||||||
chr4:56371324
|
G | A | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.861+127C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56371324 | ||||||
chr4:56371773
|
A | G | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.669-130T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371773 | ||||||
chr4:56371789
|
C | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0209 | 4 | HG01243.hp2 HG02109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-146G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371789 | ||||||
chr4:56371811
|
C | A | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.669-168G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371811 | ||||||
chr4:56371856
|
A | T | 1 | a0002c0002t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.669-213T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371856 | ||||||
chr4:56371858
|
CAG | C | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-217_669-216del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371858 | ||||||
chr4:56371898
|
A | G | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.669-255T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371898 | ||||||
chr4:56371941
|
T | TA | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.669-299dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371941 | ||||||
chr4:56371986
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0157 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.669-343G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371986 | ||||||
chr4:56371994
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.669-351G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371994 | ||||||
chr4:56372019
|
C | G | 3 | a0004c0004t0001g0008a0004c0004t0001g0129a0004c0025t0001g0126 | 5 | NA18939.hp1 NA18941.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-376G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372019 | ||||||
chr4:56372059
|
T | C | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.669-416A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372059 | ||||||
chr4:56372070
|
C | T | 1 | a0001c0005t0001g0301 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.669-427G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372070 | ||||||
chr4:56372472
|
A | T | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0018c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-829T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372472 | ||||||
chr4:56372514
|
A | G | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.669-871T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372514 | ||||||
chr4:56372643
|
T | C | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.669-1000A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372643 | ||||||
chr4:56372666
|
TAA | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1025_669-1024d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372666 | ||||||
chr4:56372727
|
T | A | 1 | a0006c0009t0004g0029 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.669-1084A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372727 | ||||||
chr4:56372752
|
TATA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-1112_669-1110d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372752 | ||||||
chr4:56372979
|
T | C | 1 | a0003c0003t0002g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.669-1336A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372979 | ||||||
chr4:56373014
|
C | T | 212 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(209): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.669-1371G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373014 | ||||||
chr4:56373112
|
G | A | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669-1469C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373112 | ||||||
chr4:56373213
|
C | CCCAAGTT others(3): Show |
1 | a0004c0004t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.669-1571_669-1570i others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373213 | ||||||
chr4:56373214
|
A | G | 1 | a0004c0004t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.669-1571T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373214 | ||||||
chr4:56373355
|
C | T | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.669-1712G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373355 | ||||||
chr4:56373433
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1790C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373433 | ||||||
chr4:56373434
|
C | T | 1 | a0007c0008t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.669-1791G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373434 | ||||||
chr4:56373459
|
G | A | 53 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(50): Show | 56 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.669-1816C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373459 | ||||||
chr4:56373614
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-1971G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373614 | ||||||
chr4:56373825
|
GTT | G | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.669-2184_669-2183d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373825 | ||||||
chr4:56373828
|
C | G | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.669-2185G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373828 | ||||||
chr4:56373832
|
T | A | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.669-2189A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373832 | ||||||
chr4:56373833
|
A | AT | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.669-2191_669-2190i others(3): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373833 | ||||||
chr4:56373835
|
T | C | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.669-2192A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373835 | ||||||
chr4:56374011
|
C | G | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.669-2368G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374011 | ||||||
chr4:56374215
|
C | CTAAAACT others(371): Show |
1 | a0005c0007t0003g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.669-2573_669-2572i others(380): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374215 | ||||||
chr4:56374367
|
C | CA | 103 | a0001c0001t0001g0166a0001c0005t0001g0285a0001c0005t0001g0313others(100): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.669-2725dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | ||||||
chr4:56374367
|
C | CAA | 22 | a0003c0003t0001g0220a0003c0003t0002g0044a0003c0003t0002g0045others(19): Show | 22 | HG00423.hp1 HG01255.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.669-2725_669-2724i others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | ||||||
chr4:56374367
|
C | CAAAAAAA | 5 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0036others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.669-2725_669-2724i others(9): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | ||||||
chr4:56374367
|
CAGAAAAA others(8): Show |
C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.669-2739_669-2725d others(17): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | ||||||
chr4:56374369
|
G | A | 174 | a0001c0001t0001g0166a0001c0005t0001g0011a0001c0005t0001g0028others(171): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.669-2726C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374369 | ||||||
chr4:56374390
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.669-2747T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374390 | ||||||
chr4:56374565
|
T | C | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-2922A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374565 | ||||||
chr4:56374606
|
AT | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-2964delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374606 | ||||||
chr4:56374694
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.669-3051G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374694 | ||||||
chr4:56374786
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.669-3143C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374786 | ||||||
chr4:56374989
|
G | A | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.668+3159C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374989 | ||||||
chr4:56375105
|
G | A | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.668+3043C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375105 | ||||||
chr4:56375143
|
G | A | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.668+3005C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375143 | ||||||
chr4:56375182
|
T | C | 1 | a0001c0005t0001g0314 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.668+2966A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375182 | ||||||
chr4:56375192
|
A | T | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.668+2956T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375192 | ||||||
chr4:56375196
|
T | C | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.668+2952A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375196 | ||||||
chr4:56375373
|
T | C | 1 | a0001c0005t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668+2775A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375373 | ||||||
chr4:56375476
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.668+2672T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375476 | ||||||
chr4:56375611
|
G | A | 10 | a0002c0002t0001g0226a0002c0002t0001g0235a0005c0007t0003g0033others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.668+2537C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375611 | ||||||
chr4:56375766
|
T | C | 1 | a0003c0003t0002g0278 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.668+2382A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375766 | ||||||
chr4:56375832
|
T | G | 114 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.668+2316A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375832 | ||||||
chr4:56375888
|
C | T | 2 | a0004c0004t0001g0132a0004c0004t0001g0133 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.668+2260G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375888 | ||||||
chr4:56376019
|
C | CT | 70 | a0001c0001t0001g0069a0001c0005t0001g0316a0001c0005t0001g0317others(67): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.668+2128dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | ||||||
chr4:56376019
|
C | CTT | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.668+2127_668+2128d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | ||||||
chr4:56376019
|
C | CTTT | 26 | a0001c0005t0001g0285a0001c0005t0001g0299a0001c0005t0001g0300others(23): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.668+2126_668+2128d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | ||||||
chr4:56376019
|
CT | C | 25 | a0001c0001t0001g0066a0001c0001t0001g0093a0001c0001t0001g0096others(22): Show | 25 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.668+2128delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | ||||||
chr4:56376055
|
G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.668+2093C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376055 | ||||||
chr4:56376084
|
T | C | 2 | a0004c0004t0001g0173a0004c0004t0001g0223 | 2 | NA18982.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.668+2064A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376084 | ||||||
chr4:56376105
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.668+2043G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376105 | ||||||
chr4:56376105
|
C | T | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.668+2043G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376105 | ||||||
chr4:56376216
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1932C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376216 | ||||||
chr4:56376411
|
T | C | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.668+1737A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376411 | ||||||
chr4:56376416
|
T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1732A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376416 | ||||||
chr4:56376434
|
G | A | 1 | a0014c0016t0001g0218 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.668+1714C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376434 | ||||||
chr4:56376464
|
A | G | 1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.668+1684T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376464 | ||||||
chr4:56376538
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1610A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376538 | ||||||
chr4:56376728
|
T | C | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+1420A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376728 | ||||||
chr4:56376772
|
G | A | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.668+1376C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376772 | ||||||
chr4:56376794
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1354T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376794 | ||||||
chr4:56376805
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.668+1343G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376805 | ||||||
chr4:56376924
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.668+1224C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376924 | ||||||
chr4:56377062
|
G | A | 1 | a0008c0011t0002g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.668+1086C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377062 | ||||||
chr4:56377066
|
CA | C | 51 | a0001c0001t0001g0125a0001c0001t0001g0166a0004c0004t0001g0005others(48): Show | 59 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.668+1081delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377066 | ||||||
chr4:56377066
|
CAA | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1080_668+1081d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377066 | ||||||
chr4:56377070
|
A | AAT | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.668+1077_668+1078i others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377070 | ||||||
chr4:56377074
|
A | T | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.668+1074T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377074 | ||||||
chr4:56377077
|
A | AAT | 44 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.668+1070_668+1071i others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377077 | ||||||
chr4:56377077
|
A | T | 1 | a0001c0005t0001g0298 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.668+1071T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377077 | ||||||
chr4:56377078
|
A | AAAT | 84 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(81): Show | 95 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(92): Show |
intron_variant | MODIFIER | c.668+1069_668+1070i others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377078 | ||||||
chr4:56377078
|
A | T | 125 | a0001c0001t0001g0068a0001c0001t0001g0125a0002c0002t0001g0115others(122): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.668+1070T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377078 | ||||||
chr4:56377082
|
T | A | 1 | a0001c0001t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.668+1066A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377082 | ||||||
chr4:56377086
|
T | TA | 202 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(199): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.668+1061dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377086 | ||||||
chr4:56377090
|
TA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1057delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377090 | ||||||
chr4:56377096
|
A | T | 1 | a0002c0002t0001g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.668+1052T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377096 | ||||||
chr4:56377101
|
A | AAAATT | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+1042_668+1046d others(7): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377101 | ||||||
chr4:56377101
|
A | T | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.668+1047T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377101 | ||||||
chr4:56377164
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.668+984A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377164 | ||||||
chr4:56377506
|
C | T | 48 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(45): Show | 55 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.668+642G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377506 | ||||||
chr4:56377578
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+570A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377578 | ||||||
chr4:56377708
|
A | G | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.668+440T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377708 | ||||||
chr4:56377779
|
T | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.668+369A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377779 | ||||||
chr4:56377949
|
C | T | 7 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.668+199G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377949 | ||||||
chr4:56377958
|
A | G | 1 | a0004c0025t0001g0126 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.668+190T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377958 | ||||||
chr4:56378052
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+96G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56378052 | ||||||
chr4:56378653
|
A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-189T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378653 | ||||||
chr4:56378653
|
A | G | 203 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(200): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.352-189T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378653 | ||||||
chr4:56378758
|
CTG | C | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.352-296_352-295del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378758 | ||||||
chr4:56378785
|
GT | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-322delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378785 | ||||||
chr4:56378881
|
T | A | 3 | a0001c0005t0001g0319a0006c0009t0004g0029a0006c0009t0004g0331 | 4 | HG02257.hp1 HG02258.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-417A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378881 | ||||||
chr4:56378889
|
A | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-425T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378889 | ||||||
chr4:56378890
|
T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-426A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378890 | ||||||
chr4:56378893
|
T | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.352-429A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378893 | ||||||
chr4:56378906
|
C | T | 1 | a0004c0004t0001g0150 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.352-442G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378906 | ||||||
chr4:56378923
|
A | C | 1 | a0003c0003t0002g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.352-459T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378923 | ||||||
chr4:56378970
|
G | A | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.352-506C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378970 | ||||||
chr4:56379040
|
C | T | 1 | a0004c0004t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.352-576G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379040 | ||||||
chr4:56379071
|
C | T | 208 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(205): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.352-607G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379071 | ||||||
chr4:56379249
|
T | G | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.352-785A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379249 | ||||||
chr4:56379340
|
C | G | 7 | a0003c0003t0002g0025a0003c0003t0002g0026a0003c0003t0002g0251others(4): Show | 9 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-876G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379340 | ||||||
chr4:56379525
|
T | G | 1 | a0002c0002t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.352-1061A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379525 | ||||||
chr4:56379532
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1068T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379532 | ||||||
chr4:56379725
|
C | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.352-1261G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379725 | ||||||
chr4:56379801
|
T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1337A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379801 | ||||||
chr4:56379853
|
G | A | 69 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.352-1389C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379853 | ||||||
chr4:56379965
|
C | G | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.352-1501G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379965 | ||||||
chr4:56380143
|
G | T | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.352-1679C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56380143 | ||||||
chr4:56380241
|
G | T | 3 | a0003c0003t0002g0238a0003c0003t0002g0250a0003c0003t0002g0295 | 3 | HG01258.hp1 HG02451.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.352-1777C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56380241 | ||||||
chr4:56380510
|
G | T | 2 | a0002c0002t0001g0178a0002c0002t0001g0179 | 2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.351+1967C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56380510 | ||||||
chr4:56381039
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+1438G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381039 | ||||||
chr4:56381157
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+1320G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381157 | ||||||
chr4:56381160
|
A | C | 1 | a0001c0005t0001g0242 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.351+1317T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381160 | ||||||
chr4:56381180
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.351+1297G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381180 | ||||||
chr4:56381423
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351+1054G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381423 | ||||||
chr4:56381452
|
C | A | 1 | a0002c0002t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.351+1025G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381452 | ||||||
chr4:56381469
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.351+1008A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381469 | ||||||
chr4:56381509
|
C | T | 1 | a0017c0022t0001g0109 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.351+968G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381509 | ||||||
chr4:56381584
|
C | CA | 19 | a0001c0001t0001g0283a0001c0005t0001g0284a0002c0002t0001g0123others(16): Show | 19 | HG01070.hp2 HG01175.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.351+892dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381584 | ||||||
chr4:56381584
|
C | CAA | 43 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(40): Show | 46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.351+891_351+892dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381584 | ||||||
chr4:56381646
|
T | TTC | 39 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(36): Show | 42 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.351+829_351+830dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381646 | ||||||
chr4:56381649
|
T | TCA | 7 | a0001c0001t0001g0057a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01109.hp2 HG03098.hp1 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+826_351+827dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCACACAC others(5): Show |
1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.351+816_351+827dup others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCACACAC others(7): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG02965.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.351+814_351+827dup others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCACACAC others(9): Show |
2 | a0001c0001t0001g0015a0001c0010t0001g0281 | 3 | HG02809.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.351+812_351+827dup others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCACACAC others(11): Show |
2 | a0002c0002t0001g0108a0003c0003t0002g0277 | 2 | HG00738.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.351+810_351+827dup others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCACACAC others(13): Show |
3 | a0002c0002t0001g0018a0002c0002t0001g0113a0002c0002t0001g0124 | 4 | NA18952.hp2 NA18973.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+808_351+827dup others(20): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(3): Show |
42 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0023others(39): Show | 50 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(5): Show |
24 | a0001c0001t0001g0125a0002c0002t0001g0201a0002c0002t0001g0202others(21): Show | 26 | HG01192.hp1 HG01891.hp2 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(7): Show |
37 | a0002c0002t0001g0207a0002c0002t0001g0214a0003c0003t0002g0240others(34): Show | 43 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(9): Show |
33 | a0002c0002t0001g0215a0002c0002t0001g0216a0003c0003t0002g0010others(30): Show | 37 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(10): Show |
1 | a0004c0004t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(17): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(11): Show |
31 | a0002c0002t0001g0106a0002c0002t0001g0107a0003c0003t0002g0027others(28): Show | 32 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(13): Show |
20 | a0002c0002t0001g0017a0002c0002t0001g0105a0002c0002t0001g0110others(17): Show | 24 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(20): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(15): Show |
9 | a0002c0002t0001g0019a0002c0002t0001g0114a0002c0002t0001g0115others(6): Show | 10 | HG01123.hp1 HG01496.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(22): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(17): Show |
3 | a0002c0002t0001g0122a0002c0002t0001g0123a0006c0009t0004g0029 | 4 | HG02257.hp1 HG02258.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(24): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCACAC others(15): Show |
1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+827_351+828ins others(22): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCTCAC others(3): Show |
6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCTCAC others(5): Show |
1 | a0005c0007t0003g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCTCAC others(7): Show |
1 | a0004c0004t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCTCAC others(9): Show |
1 | a0005c0007t0003g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381649
|
T | TCTCTCAC others(19): Show |
1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.351+827_351+828ins others(26): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | ||||||
chr4:56381653
|
A | T | 1 | a0003c0003t0002g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+824T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381653 | ||||||
chr4:56381696
|
A | G | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.351+781T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381696 | ||||||
chr4:56381742
|
A | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0157 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.351+735T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381742 | ||||||
chr4:56381976
|
G | GTC | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+499_351+500dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381976 | ||||||
chr4:56382171
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+306G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382171 | ||||||
chr4:56382253
|
G | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+224C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382253 | ||||||
chr4:56382254
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+223G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382254 | ||||||
chr4:56382411
|
G | A | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.351+66C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382411 | ||||||
chr4:56382425
|
A | G | 45 | a0002c0002t0001g0002a0002c0002t0001g0023a0002c0002t0001g0177others(42): Show | 51 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.351+52T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382425 | ||||||
chr4:56382624
|
T | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-27A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382624 | ||||||
chr4:56382690
|
T | C | 1 | a0016c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.231-93A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382690 | ||||||
chr4:56382776
|
C | T | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.231-179G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382776 | ||||||
chr4:56382792
|
G | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.231-195C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382792 | ||||||
chr4:56382836
|
G | C | 158 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(155): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.231-239C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382836 | ||||||
chr4:56382836
|
G | T | 1 | a0003c0003t0002g0286 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.231-239C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382836 | ||||||
chr4:56382926
|
G | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.231-329C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382926 | ||||||
chr4:56382974
|
T | C | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231-377A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382974 | ||||||
chr4:56382982
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-385C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382982 | ||||||
chr4:56382988
|
C | T | 3 | a0007c0008t0001g0059a0007c0008t0001g0060a0007c0008t0001g0061 | 3 | HG03041.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.231-391G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382988 | ||||||
chr4:56383016
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231-419G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383016 | ||||||
chr4:56383109
|
T | A | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.231-512A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383109 | ||||||
chr4:56383129
|
A | C | 90 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(87): Show | 102 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.231-532T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383129 | ||||||
chr4:56383162
|
A | AT | 70 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(67): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.231-566dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383162 | ||||||
chr4:56383200
|
T | C | 1 | a0002c0002t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231-603A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383200 | ||||||
chr4:56383219
|
C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-622G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383219 | ||||||
chr4:56383225
|
A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-628T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383225 | ||||||
chr4:56383226
|
C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-629G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383226 | ||||||
chr4:56383227
|
A | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-630T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383227 | ||||||
chr4:56383234
|
A | G | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-637T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383234 | ||||||
chr4:56383245
|
A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-648T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383245 | ||||||
chr4:56383248
|
T | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-651A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383248 | ||||||
chr4:56383254
|
A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-657T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383254 | ||||||
chr4:56383256
|
A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-659T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383256 | ||||||
chr4:56383278
|
G | A | 4 | a0001c0010t0001g0280a0001c0010t0001g0281a0007c0008t0001g0326others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-681C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383278 | ||||||
chr4:56383322
|
C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-725G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383322 | ||||||
chr4:56383323
|
A | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-726T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383323 | ||||||
chr4:56383324
|
C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-727G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383324 | ||||||
chr4:56383362
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+708G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383362 | ||||||
chr4:56383364
|
G | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+706C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383364 | ||||||
chr4:56383365
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+705G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383365 | ||||||
chr4:56383366
|
C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+704G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383366 | ||||||
chr4:56383368
|
C | G | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+702G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383368 | ||||||
chr4:56383370
|
G | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+700C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383370 | ||||||
chr4:56383372
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+698G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383372 | ||||||
chr4:56383373
|
T | G | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+697A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383373 | ||||||
chr4:56383376
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+694G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383376 | ||||||
chr4:56383377
|
A | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+693T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383377 | ||||||
chr4:56383564
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.230+506G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383564 | ||||||
chr4:56383584
|
G | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.230+486C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383584 | ||||||
chr4:56383765
|
A | T | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.230+305T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383765 | ||||||
chr4:56383777
|
T | C | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.230+293A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383777 | ||||||
chr4:56383845
|
T | C | 1 | a0001c0005t0001g0320 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.230+225A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383845 | ||||||
chr4:56383918
|
T | TA | 260 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(257): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.230+151_230+152ins others(1): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383918 | ||||||
chr4:56384657
|
TA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-317delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384657 | ||||||
chr4:56384702
|
A | T | 1 | a0004c0004t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-42-361T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384702 | ||||||
chr4:56384702
|
AT | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-42-362delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384702 | ||||||
chr4:56384795
|
C | T | 4 | a0003c0003t0002g0243a0003c0003t0002g0244a0003c0003t0002g0245others(1): Show | 4 | HG00609.hp2 HG02083.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-454G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384795 | ||||||
chr4:56385027
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-686G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385027 | ||||||
chr4:56385331
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-990A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385331 | ||||||
chr4:56385348
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1007A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385348 | ||||||
chr4:56385352
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1011A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385352 | ||||||
chr4:56385353
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1012A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385353 | ||||||
chr4:56385354
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1013G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385354 | ||||||
chr4:56385356
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1015G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385356 | ||||||
chr4:56385357
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1016A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385357 | ||||||
chr4:56385358
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1017A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385358 | ||||||
chr4:56385362
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1021G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385362 | ||||||
chr4:56385363
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1022A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385363 | ||||||
chr4:56385364
|
G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1023C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385364 | ||||||
chr4:56385369
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1028A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385369 | ||||||
chr4:56385374
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1033A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385374 | ||||||
chr4:56385376
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1035A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385376 | ||||||
chr4:56385377
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1036A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385377 | ||||||
chr4:56385379
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1038G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385379 | ||||||
chr4:56385382
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1041G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385382 | ||||||
chr4:56385383
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1042A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385383 | ||||||
chr4:56385384
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1043G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385384 | ||||||
chr4:56385387
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1046A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385387 | ||||||
chr4:56385391
|
G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1050C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385391 | ||||||
chr4:56385392
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1051G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385392 | ||||||
chr4:56385394
|
G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1053C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385394 | ||||||
chr4:56385395
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1054A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385395 | ||||||
chr4:56385397
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1056A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385397 | ||||||
chr4:56385398
|
A | T | 2 | a0006c0009t0004g0029a0006c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-42-1057T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385398 | ||||||
chr4:56385399
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1058A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385399 | ||||||
chr4:56385400
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1059G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385400 | ||||||
chr4:56385403
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1062A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385403 | ||||||
chr4:56385405
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1064G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385405 | ||||||
chr4:56385408
|
T | G | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1067A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385408 | ||||||
chr4:56385414
|
C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1073G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385414 | ||||||
chr4:56385415
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1074A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385415 | ||||||
chr4:56385417
|
G | GAGAAAGA others(7): Show |
1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1077_-42-1076i others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385417 | ||||||
chr4:56385496
|
A | T | 26 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(23): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42-1155T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385496 | ||||||
chr4:56385679
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0168 | 4 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-1338G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385679 | ||||||
chr4:56385707
|
C | T | 48 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(45): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.-42-1366G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385707 | ||||||
chr4:56385779
|
A | AT | 65 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(62): Show | 71 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-42-1439dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385779 | ||||||
chr4:56385929
|
CT | C | 8 | a0001c0001t0001g0103a0002c0002t0001g0124a0002c0002t0001g0217others(5): Show | 8 | HG01943.hp1 HG01993.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1432delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385929 | ||||||
chr4:56385932
|
T | TC | 112 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(109): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-43+1429_-43+1430i others(3): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385932 | ||||||
chr4:56385933
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-43+1429A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385933 | ||||||
chr4:56385948
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1414T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385948 | ||||||
chr4:56385972
|
C | T | 1 | a0004c0004t0001g0169 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-43+1390G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385972 | ||||||
chr4:56385978
|
T | C | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-43+1384A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385978 | ||||||
chr4:56386143
|
T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1219A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386143 | ||||||
chr4:56386332
|
C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1030G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386332 | ||||||
chr4:56386469
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43+893G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386469 | ||||||
chr4:56386522
|
G | A | 11 | a0004c0004t0001g0005a0004c0004t0001g0022a0004c0004t0001g0169others(8): Show | 15 | HG00408.hp1 HG02015.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+840C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386522 | ||||||
chr4:56386712
|
C | G | 212 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(209): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-43+650G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386712 | ||||||
chr4:56386720
|
G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+642C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386720 | ||||||
chr4:56386775
|
G | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.-43+587C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386775 | ||||||
chr4:56386799
|
C | CA | 108 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0001g0158others(105): Show | 124 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-43+562dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
C | CAA | 19 | a0002c0002t0001g0226a0002c0002t0001g0227a0002c0002t0001g0232others(16): Show | 20 | HG02080.hp1 HG02559.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43+561_-43+562dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
C | CAAA | 8 | a0003c0003t0002g0238a0003c0003t0002g0239a0005c0007t0003g0033others(5): Show | 8 | HG00323.hp2 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+560_-43+562dup others(3): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
C | CAAAA | 52 | a0001c0001t0001g0283a0001c0005t0001g0242a0001c0010t0001g0280others(49): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.-43+559_-43+562dup others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
C | CAAAAA | 14 | a0001c0005t0001g0284a0001c0005t0001g0285a0003c0003t0002g0286others(11): Show | 14 | HG01070.hp2 HG01074.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43+558_-43+562dup others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
C | CAAAAAA | 26 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0298others(23): Show | 29 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-43+557_-43+562dup others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
C | CAAAAAAA | 7 | a0001c0005t0001g0032a0001c0005t0001g0321a0001c0005t0001g0322others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+556_-43+562dup others(7): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+562delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
CAA | C | 6 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(3): Show | 6 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+561_-43+562del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
CAAAAAA | C | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0018c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+557_-43+562del others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386799
|
CAAAAAAA others(3): Show |
C | 1 | a0004c0004t0001g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-43+553_-43+562del others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | ||||||
chr4:56386823
|
G | A | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+539C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386823 | ||||||
chr4:56386823
|
G | T | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-43+539C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386823 | ||||||
chr4:56386825
|
A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+537T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386825 | ||||||
chr4:56386875
|
A | T | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-43+487T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386875 | ||||||
chr4:56387045
|
G | A | 2 | a0003c0003t0002g0327a0003c0003t0002g0328 | 2 | HG01169.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-43+317C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56387045 | ||||||
chr4:56387202
|
T | C | 2 | a0002c0002t0001g0329a0002c0002t0007g0330 | 2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-43+160A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56387202 |