geneid | 7849 |
---|---|
ensemblid | ENSG00000125618.18 |
hgncid | 8622 |
symbol | PAX8 |
name | paired box 8 |
refseq_nuc | NM_003466.4 |
refseq_prot | NP_003457.1 |
ensembl_nuc | ENST00000429538.8 |
ensembl_prot | ENSP00000395498.3 |
mane_status | MANE Select |
chr | chr2 |
start | 113215997 |
end | 113278921 |
strand | - |
ver | v1.2 |
region | chr2:113215997-113278921 |
region5000 | chr2:113210997-113283921 |
regionname0 | PAX8_chr2_113215997_113278921 |
regionname5000 | PAX8_chr2_113210997_113283921 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 450 | 297 | 89 | 54 | 115 | 9 | 28 | 91 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0002 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0003 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0004 | 0/0 | 450 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1353 | 286 | 86 | 53 | 109 | 9 | 27 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0002 | 0/0 | 1353 | 4 | 0 | 0 | 4 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0003 | 0/0 | 1353 | 3 | 3 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0004 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0005 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0006 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0007 | 0/0 | 1353 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0008 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0009 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
c0010 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2703 | 91 | 15 | 15 | 48 | 2 | 11 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0002 | 0/0 | 2703 | 60 | 38 | 11 | 5 | 3 | 3 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0003 | 0/0 | 2703 | 45 | 1 | 4 | 35 | 2 | 3 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0004 | 0/1 | 2703 | 28 | 1 | 11 | 9 | 1 | 5 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0005 | 0/0 | 2703 | 10 | 0 | 5 | 5 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0006 | 1/0 | 2703 | 8 | 6 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0007 | 0/0 | 2703 | 8 | 1 | 1 | 4 | 0 | 2 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0008 | 0/0 | 2703 | 6 | 0 | 0 | 6 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0009 | 0/0 | 2703 | 5 | 4 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0010 | 0/0 | 2703 | 4 | 0 | 1 | 0 | 1 | 2 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0011 | 0/0 | 2703 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0012 | 0/0 | 2703 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0013 | 0/0 | 2703 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0014 | 0/0 | 2703 | 2 | 1 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0015 | 0/0 | 2703 | 2 | 1 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0016 | 0/0 | 2703 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0017 | 0/0 | 2703 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0018 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0019 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0020 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0021 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0022 | 0/0 | 2703 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0023 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0024 | 0/0 | 2703 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0025 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0026 | 0/0 | 2703 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0027 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0028 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0029 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0030 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0031 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0032 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0033 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0034 | 0/0 | 2703 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0035 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0036 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0037 | 0/0 | 2703 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
t0038 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 3 | 3 | 0 | 4 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0002 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0008 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1353 | 286 | 86 | 53 | 109 | 9 | 27 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0002 | 0/0 | 1353 | 4 | 0 | 0 | 4 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0003 | 0/0 | 1353 | 3 | 3 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0004 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0006 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0007 | 0/0 | 1353 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0009 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0002c0005 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0003c0010 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0004c0008 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4055 | 88 | 14 | 15 | 47 | 1 | 11 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0002 | 0/0 | 4055 | 59 | 38 | 11 | 4 | 3 | 3 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0003 | 0/0 | 4055 | 40 | 0 | 4 | 31 | 2 | 3 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0004 | 0/1 | 4055 | 28 | 1 | 11 | 9 | 1 | 5 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0005 | 0/0 | 4055 | 9 | 0 | 4 | 5 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0006 | 1/0 | 4055 | 8 | 6 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0007 | 0/0 | 4055 | 7 | 1 | 1 | 4 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0008 | 0/0 | 4055 | 6 | 0 | 0 | 6 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0009 | 0/0 | 4055 | 5 | 4 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0010 | 0/0 | 4055 | 4 | 0 | 1 | 0 | 1 | 2 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0011 | 0/0 | 4055 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0012 | 0/0 | 4055 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0014 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0015 | 0/0 | 4055 | 2 | 1 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0016 | 0/0 | 4055 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0017 | 0/0 | 4055 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0018 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0019 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0020 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0021 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0022 | 0/0 | 4055 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0023 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0024 | 0/0 | 4055 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0025 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0026 | 0/0 | 4055 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0027 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0028 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0029 | 0/0 | 4055 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0030 | 0/0 | 4055 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0031 | 0/0 | 4055 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0032 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0033 | 0/0 | 4055 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0034 | 0/0 | 4055 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0035 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0036 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0037 | 0/0 | 4055 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0001t0038 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0002t0003 | 0/0 | 4055 | 4 | 0 | 0 | 4 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0003t0003 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0003t0013 | 0/0 | 4055 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0004t0007 | 0/0 | 4055 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0006t0002 | 0/0 | 4055 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0007t0005 | 0/0 | 4055 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0001c0009t0014 | 0/0 | 4055 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0002c0005t0001 | 0/0 | 4055 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0003c0010t0001 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
a0004c0008t0001 | 0/0 | 4055 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | copy fasta | chr2 | 113210997 | 113283921 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 3 | 3 | 0 | 4 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0005g0002 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0006g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0009g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0010g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0015g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0016g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0017g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0018g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0019g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0022g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0023g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0024g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0025g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0026g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0027g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0028g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0029g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0030g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0031g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0032g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0033g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0034g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0035g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0036g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0037g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0001t0038g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0002t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0003t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0003t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0004t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0006t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0007t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0001c0009t0014g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0002c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0003c0010t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
a0004c0008t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00099 | hp2 | a0001 | c0001 | t0022 | g0124 | EUR | GBR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00140 | hp1 | a0004 | c0008 | t0001 | g0048 | EUR | GBR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | GBR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | FIN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00544 | hp1 | a0001 | c0009 | t0014 | g0223 | EAS | CHS | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0150 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | CHS | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0241 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00733 | hp2 | a0001 | c0001 | t0029 | g0070 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01106 | hp2 | a0001 | c0001 | t0033 | g0239 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01168 | hp2 | a0001 | c0007 | t0005 | g0102 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01192 | hp1 | a0001 | c0001 | t0030 | g0170 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01346 | hp2 | a0001 | c0001 | t0009 | g0141 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01433 | hp2 | a0001 | c0001 | t0031 | g0209 | AMR | CLM | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01884 | hp1 | a0001 | c0001 | t0036 | g0117 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01891 | hp2 | a0001 | c0001 | t0032 | g0037 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02015 | hp2 | a0001 | c0001 | t0015 | g0098 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0057 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02257 | hp2 | a0001 | c0003 | t0013 | g0026 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02572 | hp1 | a0001 | c0001 | t0023 | g0212 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02622 | hp2 | a0001 | c0001 | t0016 | g0033 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02698 | hp2 | a0001 | c0001 | t0024 | g0250 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02723 | hp1 | a0001 | c0001 | t0038 | g0253 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02738 | hp2 | a0001 | c0001 | t0010 | g0018 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02895 | hp1 | a0001 | c0001 | t0020 | g0021 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02896 | hp1 | a0001 | c0001 | t0019 | g0030 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02976 | hp1 | a0001 | c0001 | t0017 | g0020 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02976 | hp2 | a0001 | c0003 | t0013 | g0027 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03130 | hp1 | a0001 | c0001 | t0035 | g0174 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03130 | hp2 | a0001 | c0001 | t0018 | g0028 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0023 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0236 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03239 | hp1 | a0001 | c0001 | t0026 | g0096 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03453 | hp1 | a0001 | c0001 | t0027 | g0083 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0248 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0249 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03516 | hp2 | a0003 | c0010 | t0001 | g0199 | AFR | ESN | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0097 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0126 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | STU | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | BEB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03834 | hp2 | a0001 | c0004 | t0007 | g0251 | SAS | BEB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0018 | SAS | STU | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0087 | SAS | STU | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | STU | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | CHB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | CHB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18747 | hp1 | a0001 | c0001 | t0007 | g0213 | EAS | CHB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | CHB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0111 | AFR | YRI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0121 | AFR | YRI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18954 | hp1 | a0002 | c0005 | t0001 | g0201 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18963 | hp2 | a0001 | c0001 | t0008 | g0168 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18982 | hp2 | a0001 | c0001 | t0037 | g0157 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18989 | hp2 | a0001 | c0006 | t0002 | g0101 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18994 | hp2 | a0001 | c0001 | t0008 | g0184 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19010 | hp1 | a0001 | c0001 | t0008 | g0045 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19030 | hp1 | a0001 | c0001 | t0016 | g0232 | AFR | LWK | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19065 | hp1 | a0001 | c0001 | t0034 | g0245 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19068 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19090 | hp2 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | YRI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | YRI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0020 | AFR | ASW | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ASW | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0056 | EUR | TSI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0238 | EUR | TSI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20805 | hp2 | a0001 | c0001 | t0010 | g0179 | EUR | TSI | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0025 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0024 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | JPT | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | USA | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA20300 | hp2 | a0001 | c0001 | t0021 | g0029 | AFR | USA | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA21309 | hp1 | a0001 | c0001 | t0025 | g0246 | AFR | LWK | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0142 | REF | REF | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0235 | REF | REF | PAX8_chr2_113210997_113283921 | PAX8 | chr2 | 113210997 | 113283921 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113235496
|
A | G | 1 | a0004 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.985T>C | p.Phe329Leu | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/12 | 1151/4055 | 985/1353 | 329/450 | chr2 | 113235496 | ||
chr2:113242030
|
G | C | 1 | a0003 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.579C>G | p.Ser193Arg | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 6/12 | 745/4055 | 579/1353 | 193/450 | chr2 | 113242030 | ||
chr2:113242726
|
C | T | 1 | a0002 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.442G>A | p.Val148Met | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/12 | 608/4055 | 442/1353 | 148/450 | chr2 | 113242726 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113227201
|
G | A | 1 | a0001c0003 | 3 | HG02257.hp2 HG02976.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1143C>T | p.Ser381Ser | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/12 | 1309/4055 | 1143/1353 | 381/450 | chr2 | 113227201 | ||
chr2:113227228
|
G | A | 1 | a0001c0009 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.1116C>T | p.Pro372Pro | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/12 | 1282/4055 | 1116/1353 | 372/450 | chr2 | 113227228 | ||
chr2:113241623
|
C | T | 1 | a0001c0007 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.705G>A | p.Pro235Pro | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/12 | 871/4055 | 705/1353 | 235/450 | chr2 | 113241623 | ||
chr2:113242105
|
C | T | 1 | a0001c0006 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.504G>A | p.Pro168Pro | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 6/12 | 670/4055 | 504/1353 | 168/450 | chr2 | 113242105 | ||
chr2:113244585
|
C | T | 1 | a0001c0004 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.231G>A | p.Gly77Gly | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/12 | 397/4055 | 231/1353 | 77/450 | chr2 | 113244585 | ||
chr2:113246816
|
C | T | 1 | a0001c0002 | 4 | NA18945.hp2 NA18955.hp2 NA18956.hp1 others(1): Show |
synonymous_variant | LOW | c.129G>A | p.Arg43Arg | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/12 | 295/4055 | 129/1353 | 43/450 | chr2 | 113246816 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113216055
|
G | A | 15 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(12): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2478C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 2478 | chr2 | 113216055 | |||||
chr2:113216156
|
G | T | 1 | a0001c0001t0030 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2377C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 2377 | chr2 | 113216156 | |||||
chr2:113216224
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*2309A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 2309 | chr2 | 113216224 | |||||
chr2:113216257
|
C | T | 1 | a0001c0001t0034 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2276G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 2276 | chr2 | 113216257 | |||||
chr2:113216387
|
T | C | 15 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(12): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2146A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 2146 | chr2 | 113216387 | |||||
chr2:113216388
|
G | A | 1 | a0001c0001t0031 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 2145 | chr2 | 113216388 | |||||
chr2:113216560
|
C | T | 1 | a0001c0001t0029 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1973G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1973 | chr2 | 113216560 | |||||
chr2:113216619
|
G | C | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(16): Show | 132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1914C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1914 | chr2 | 113216619 | |||||
chr2:113216726
|
G | C | 1 | a0001c0001t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1807C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1807 | chr2 | 113216726 | |||||
chr2:113216768
|
C | T | 1 | a0001c0001t0033 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1765G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1765 | chr2 | 113216768 | |||||
chr2:113216818
|
G | A | 1 | a0001c0001t0017 | 2 | HG02976.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1715C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1715 | chr2 | 113216818 | |||||
chr2:113217489
|
T | G | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(16): Show | 95 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1044A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1044 | chr2 | 113217489 | |||||
chr2:113217527
|
T | G | 20 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(17): Show | 96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1006A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1006 | chr2 | 113217527 | |||||
chr2:113217533
|
A | G | 5 | a0001c0001t0004a0001c0001t0008a0001c0001t0026others(2): Show | 37 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 1000 | chr2 | 113217533 | |||||
chr2:113217581
|
A | T | 1 | a0001c0001t0025 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 952 | chr2 | 113217581 | |||||
chr2:113217688
|
C | T | 1 | a0001c0001t0024 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 845 | chr2 | 113217688 | |||||
chr2:113217831
|
G | A | 1 | a0001c0001t0035 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*702C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 702 | chr2 | 113217831 | |||||
chr2:113217906
|
A | T | 2 | a0001c0001t0023a0001c0001t0038 | 2 | HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*627T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 627 | chr2 | 113217906 | |||||
chr2:113218055
|
T | C | 1 | a0001c0003t0013 | 2 | HG02257.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*478A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 478 | chr2 | 113218055 | |||||
chr2:113218064
|
C | A | 1 | a0001c0001t0036 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 469 | chr2 | 113218064 | |||||
chr2:113218090
|
G | T | 1 | a0001c0001t0018 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 443 | chr2 | 113218090 | |||||
chr2:113218197
|
C | A | 1 | a0001c0001t0037 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 336 | chr2 | 113218197 | |||||
chr2:113218243
|
C | T | 1 | a0001c0001t0022 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*290G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 290 | chr2 | 113218243 | |||||
chr2:113218346
|
T | C | 1 | a0001c0001t0010 | 4 | HG00642.hp1 HG02738.hp2 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*187A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 12/12 | 187 | chr2 | 113218346 | |||||
chr2:113278421
|
G | A | 1 | a0001c0001t0038 | 1 | HG02723.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-27C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/12 | chr2 | 113278421 | ||||||
chr2:113278859
|
C | G | 7 | a0001c0001t0011a0001c0001t0012a0001c0001t0018others(4): Show | 10 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-104G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 1/12 | 465 | chr2 | 113278859 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113218743
|
G | A | 1 | a0001c0001t0037g0157 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1277-134C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 11/11 | chr2 | 113218743 | ||||||
chr2:113219011
|
T | C | 1 | a0001c0001t0004g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1277-402A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 11/11 | chr2 | 113219011 | ||||||
chr2:113219255
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1277-646C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 11/11 | chr2 | 113219255 | ||||||
chr2:113219505
|
T | C | 1 | a0001c0001t0004g0046 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1276+587A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 11/11 | chr2 | 113219505 | ||||||
chr2:113219877
|
G | A | 58 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(55): Show | 65 | HG00323.hp2 HG00673.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.1276+215C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 11/11 | chr2 | 113219877 | ||||||
chr2:113220039
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1276+53G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 11/11 | chr2 | 113220039 | ||||||
chr2:113220285
|
T | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(248): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1190-107A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220285 | ||||||
chr2:113220305
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0173a0001c0001t0001g0175others(1): Show | 6 | HG01891.hp1 HG02630.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-127G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220305 | ||||||
chr2:113220306
|
G | A | 6 | a0001c0001t0009g0031a0001c0001t0009g0119a0001c0001t0009g0120others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-128C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220306 | ||||||
chr2:113220357
|
A | G | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1190-179T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220357 | ||||||
chr2:113220359
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(79): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1190-181G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220359 | ||||||
chr2:113220606
|
A | G | 26 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(23): Show | 32 | HG00323.hp2 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1190-428T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220606 | ||||||
chr2:113220645
|
G | C | 1 | a0001c0001t0010g0150 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1190-467C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220645 | ||||||
chr2:113220711
|
T | A | 2 | a0001c0001t0023g0212a0001c0001t0038g0253 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1190-533A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220711 | ||||||
chr2:113220747
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1190-569C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220747 | ||||||
chr2:113220944
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1190-766C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113220944 | ||||||
chr2:113221073
|
C | T | 112 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(109): Show | 129 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1190-895G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221073 | ||||||
chr2:113221191
|
A | G | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1190-1013T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221191 | ||||||
chr2:113221248
|
G | A | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-1070C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221248 | ||||||
chr2:113221284
|
C | CCTCA | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-1107_1190-110 others(8): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221284 | ||||||
chr2:113221285
|
T | G | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-1107A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221285 | ||||||
chr2:113221288
|
G | C | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-1110C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221288 | ||||||
chr2:113221329
|
C | T | 25 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(22): Show | 31 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1190-1151G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221329 | ||||||
chr2:113221363
|
C | G | 112 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(109): Show | 129 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1190-1185G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221363 | ||||||
chr2:113221387
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0032g0037 | 2 | HG01891.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1190-1209C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221387 | ||||||
chr2:113221434
|
T | C | 1 | a0001c0002t0003g0017 | 2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1190-1256A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221434 | ||||||
chr2:113221583
|
A | G | 37 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(34): Show | 43 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1190-1405T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221583 | ||||||
chr2:113221660
|
T | G | 1 | a0001c0001t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1190-1482A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221660 | ||||||
chr2:113221662
|
A | T | 1 | a0001c0001t0002g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1190-1484T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221662 | ||||||
chr2:113221778
|
G | C | 1 | a0001c0001t0004g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1190-1600C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221778 | ||||||
chr2:113221787
|
G | A | 9 | a0001c0001t0002g0014a0001c0001t0002g0034a0001c0001t0002g0089others(6): Show | 10 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1190-1609C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221787 | ||||||
chr2:113221833
|
C | T | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-1655G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221833 | ||||||
chr2:113221856
|
C | T | 2 | a0001c0001t0006g0081a0001c0001t0006g0082 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1190-1678G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221856 | ||||||
chr2:113221857
|
G | A | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-1679C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221857 | ||||||
chr2:113221869
|
C | T | 26 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(23): Show | 32 | HG00323.hp2 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1190-1691G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113221869 | ||||||
chr2:113222003
|
T | A | 26 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(23): Show | 32 | HG00323.hp2 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1190-1825A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113222003 | ||||||
chr2:113222107
|
A | T | 1 | a0003c0010t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1190-1929T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113222107 | ||||||
chr2:113222542
|
C | T | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1190-2364G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113222542 | ||||||
chr2:113222612
|
G | A | 25 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(22): Show | 31 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1190-2434C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113222612 | ||||||
chr2:113222626
|
G | A | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1190-2448C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113222626 | ||||||
chr2:113222744
|
C | T | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1190-2566G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113222744 | ||||||
chr2:113223068
|
C | G | 31 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(28): Show | 32 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1190-2890G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113223068 | ||||||
chr2:113223159
|
C | T | 54 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(51): Show | 64 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-2981G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113223159 | ||||||
chr2:113223445
|
G | A | 112 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(109): Show | 129 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1190-3267C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113223445 | ||||||
chr2:113223560
|
T | C | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1190-3382A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113223560 | ||||||
chr2:113223639
|
C | G | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1190-3461G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113223639 | ||||||
chr2:113223982
|
A | G | 9 | a0001c0001t0002g0131a0001c0001t0002g0214a0001c0001t0003g0007others(6): Show | 11 | HG02132.hp1 HG03704.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.1189+3173T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113223982 | ||||||
chr2:113224007
|
T | C | 2 | a0001c0001t0023g0212a0001c0001t0038g0253 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1189+3148A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224007 | ||||||
chr2:113224213
|
A | G | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1189+2942T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224213 | ||||||
chr2:113224233
|
A | G | 160 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(157): Show | 183 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1189+2922T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224233 | ||||||
chr2:113224462
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(248): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1189+2693T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224462 | ||||||
chr2:113224463
|
C | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(79): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1189+2692G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224463 | ||||||
chr2:113224466
|
G | A | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1189+2689C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224466 | ||||||
chr2:113224547
|
C | CA | 11 | a0001c0001t0001g0165a0001c0001t0001g0202a0001c0001t0001g0252others(8): Show | 11 | HG01175.hp1 HG01175.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1189+2607dupT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224547 | ||||||
chr2:113224565
|
AG | A | 5 | a0001c0001t0004g0059a0001c0001t0004g0187a0001c0001t0018g0028others(2): Show | 5 | HG01167.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189+2589delC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224565 | ||||||
chr2:113224566
|
G | A | 110 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(107): Show | 127 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1189+2589C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224566 | ||||||
chr2:113224723
|
G | C | 1 | a0001c0001t0006g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1189+2432C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224723 | ||||||
chr2:113224780
|
G | A | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1189+2375C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224780 | ||||||
chr2:113224814
|
AATAAAAA others(18): Show |
A | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1189+2316_1189+234 others(29): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224814 | ||||||
chr2:113224836
|
AAATATAA others(3): Show |
A | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189+2309_1189+231 others(14): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224836 | ||||||
chr2:113224839
|
T | TATAAAAT others(3): Show |
1 | a0001c0001t0024g0250 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1189+2306_1189+231 others(14): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224839 | ||||||
chr2:113224839
|
TATAAA | T | 82 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(79): Show | 97 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1189+2311_1189+231 others(9): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224839 | ||||||
chr2:113224839
|
TATAAAAT others(3): Show |
T | 4 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0006g0224others(1): Show | 6 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189+2306_1189+231 others(14): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224839 | ||||||
chr2:113224839
|
TATAAAAT others(8): Show |
T | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1189+2301_1189+231 others(19): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224839 | ||||||
chr2:113224839
|
TATAAAAT others(13): Show |
T | 26 | a0001c0001t0002g0085a0001c0001t0003g0008a0001c0001t0003g0009others(23): Show | 32 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1189+2296_1189+231 others(24): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224839 | ||||||
chr2:113224839
|
TATAAAAT others(18): Show |
T | 1 | a0001c0001t0001g0164 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1189+2291_1189+231 others(29): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113224839 | ||||||
chr2:113225007
|
T | C | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1189+2148A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225007 | ||||||
chr2:113225031
|
G | A | 33 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1189+2124C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225031 | ||||||
chr2:113225114
|
A | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0208 | 2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1189+2041T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225114 | ||||||
chr2:113225185
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1189+1970C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225185 | ||||||
chr2:113225385
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1189+1770G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225385 | ||||||
chr2:113225441
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1189+1714T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225441 | ||||||
chr2:113225556
|
C | T | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1189+1599G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225556 | ||||||
chr2:113225790
|
G | A | 7 | a0001c0001t0004g0011a0001c0001t0004g0038a0001c0001t0004g0041others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189+1365C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225790 | ||||||
chr2:113225814
|
A | G | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1189+1341T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113225814 | ||||||
chr2:113226360
|
T | C | 81 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(78): Show | 97 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1189+795A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226360 | ||||||
chr2:113226407
|
T | C | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1189+748A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226407 | ||||||
chr2:113226456
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(79): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1189+699C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226456 | ||||||
chr2:113226669
|
G | GTCA | 108 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(105): Show | 125 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1189+483_1189+485d others(5): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226669 | ||||||
chr2:113226669
|
G | GTCATCA | 3 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0003g0136 | 3 | HG01243.hp2 HG02630.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1189+480_1189+485d others(8): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226669 | ||||||
chr2:113226726
|
T | C | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1189+429A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226726 | ||||||
chr2:113226913
|
G | C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1189+242C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226913 | ||||||
chr2:113226926
|
C | T | 47 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(44): Show | 57 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1189+229G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113226926 | ||||||
chr2:113227017
|
T | C | 37 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(34): Show | 43 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1189+138A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113227017 | ||||||
chr2:113227064
|
A | G | 2 | a0001c0001t0007g0163a0001c0001t0007g0169 | 2 | NA18946.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1189+91T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113227064 | ||||||
chr2:113227126
|
G | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0136 | 2 | NA18999.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1189+29C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 10/11 | chr2 | 113227126 | ||||||
chr2:113227280
|
G | A | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1088-24C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113227280 | ||||||
chr2:113227285
|
T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0160 | 2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1088-29A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113227285 | ||||||
chr2:113227506
|
C | G | 3 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0038g0253 | 3 | HG02572.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1088-250G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113227506 | ||||||
chr2:113227593
|
C | T | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1088-337G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113227593 | ||||||
chr2:113227609
|
C | G | 33 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1088-353G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113227609 | ||||||
chr2:113227888
|
C | A | 8 | a0001c0001t0009g0031a0001c0001t0009g0119a0001c0001t0009g0120others(5): Show | 8 | HG02257.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088-632G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113227888 | ||||||
chr2:113228415
|
CAG | C | 5 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(2): Show | 5 | HG01884.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-1161_1088-116 others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113228415 | ||||||
chr2:113228689
|
T | G | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1088-1433A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113228689 | ||||||
chr2:113228738
|
T | C | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1088-1482A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113228738 | ||||||
chr2:113228803
|
C | G | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1088-1547G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113228803 | ||||||
chr2:113228845
|
T | G | 1 | a0001c0001t0003g0140 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1088-1589A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113228845 | ||||||
chr2:113229052
|
C | T | 31 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(28): Show | 32 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1088-1796G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229052 | ||||||
chr2:113229199
|
C | G | 1 | a0001c0001t0004g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1088-1943G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229199 | ||||||
chr2:113229304
|
A | G | 37 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(34): Show | 43 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1088-2048T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229304 | ||||||
chr2:113229462
|
C | T | 5 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(2): Show | 5 | HG01884.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-2206G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229462 | ||||||
chr2:113229463
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1088-2207C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229463 | ||||||
chr2:113229488
|
C | T | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-2232G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229488 | ||||||
chr2:113229672
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1088-2416C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229672 | ||||||
chr2:113229786
|
C | T | 1 | a0001c0001t0020g0021 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1088-2530G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113229786 | ||||||
chr2:113230171
|
T | C | 1 | a0001c0001t0008g0045 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1088-2915A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230171 | ||||||
chr2:113230221
|
T | G | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1088-2965A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230221 | ||||||
chr2:113230270
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1088-3014G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230270 | ||||||
chr2:113230366
|
A | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0173a0001c0001t0001g0175others(1): Show | 6 | HG01891.hp1 HG02630.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1088-3110T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230366 | ||||||
chr2:113230470
|
C | T | 1 | a0001c0001t0038g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1088-3214G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230470 | ||||||
chr2:113230770
|
A | G | 4 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0006g0224others(1): Show | 6 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088-3514T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230770 | ||||||
chr2:113230891
|
T | C | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1088-3635A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230891 | ||||||
chr2:113230915
|
G | A | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1088-3659C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230915 | ||||||
chr2:113230926
|
G | A | 3 | a0001c0001t0023g0212a0001c0001t0032g0037a0001c0001t0038g0253 | 3 | HG01891.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1088-3670C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113230926 | ||||||
chr2:113231152
|
T | C | 37 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(34): Show | 43 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1088-3896A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231152 | ||||||
chr2:113231534
|
C | T | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1087+3860G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231534 | ||||||
chr2:113231545
|
A | AG | 123 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(120): Show | 140 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1087+3848dupC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231545 | ||||||
chr2:113231659
|
C | T | 31 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(28): Show | 32 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1087+3735G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231659 | ||||||
chr2:113231690
|
T | C | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1087+3704A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231690 | ||||||
chr2:113231750
|
T | C | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1087+3644A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231750 | ||||||
chr2:113231791
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1087+3603G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231791 | ||||||
chr2:113231853
|
C | T | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+3541G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231853 | ||||||
chr2:113231854
|
G | C | 4 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+3540C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231854 | ||||||
chr2:113231911
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1087+3483T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231911 | ||||||
chr2:113231981
|
G | A | 80 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(77): Show | 96 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1087+3413C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113231981 | ||||||
chr2:113232415
|
A | G | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+2979T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232415 | ||||||
chr2:113232438
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1087+2956G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232438 | ||||||
chr2:113232501
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1087+2893G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232501 | ||||||
chr2:113232576
|
T | G | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+2818A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232576 | ||||||
chr2:113232665
|
T | C | 30 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(27): Show | 31 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1087+2729A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232665 | ||||||
chr2:113232684
|
G | A | 111 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(108): Show | 128 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1087+2710C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232684 | ||||||
chr2:113232764
|
C | T | 1 | a0001c0001t0024g0250 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+2630G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232764 | ||||||
chr2:113232816
|
C | A | 111 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(108): Show | 128 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1087+2578G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232816 | ||||||
chr2:113232863
|
C | T | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+2531G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232863 | ||||||
chr2:113232866
|
C | T | 1 | a0001c0001t0012g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1087+2528G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232866 | ||||||
chr2:113232974
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1087+2420G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232974 | ||||||
chr2:113232978
|
C | T | 10 | a0001c0001t0002g0091a0001c0001t0002g0107a0001c0001t0002g0108others(7): Show | 11 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1087+2416G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113232978 | ||||||
chr2:113233044
|
C | CTCCCT | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+2345_1087+234 others(9): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233044 | ||||||
chr2:113233169
|
T | A | 1 | a0001c0001t0025g0246 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1087+2225A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233169 | ||||||
chr2:113233330
|
G | GA | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(224): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1087+2063dupT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233330 | ||||||
chr2:113233330
|
G | GAA | 21 | a0001c0001t0001g0146a0001c0001t0001g0165a0001c0001t0001g0173others(18): Show | 21 | HG00408.hp2 HG00733.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1087+2062_1087+206 others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233330 | ||||||
chr2:113233364
|
A | G | 23 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(20): Show | 29 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1087+2030T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233364 | ||||||
chr2:113233496
|
G | A | 13 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(10): Show | 17 | HG00639.hp2 HG01243.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1087+1898C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233496 | ||||||
chr2:113233571
|
G | A | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1087+1823C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233571 | ||||||
chr2:113233616
|
T | G | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+1778A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233616 | ||||||
chr2:113233632
|
C | A | 1 | a0001c0001t0002g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1087+1762G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233632 | ||||||
chr2:113233677
|
C | CA | 32 | a0001c0001t0001g0173a0001c0001t0001g0189a0001c0001t0001g0205others(29): Show | 38 | HG00323.hp2 HG01884.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.1087+1716dupT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233677 | ||||||
chr2:113233677
|
CAAAAAAC others(2): Show |
C | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+1708_1087+171 others(13): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233677 | ||||||
chr2:113233684
|
C | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(243): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1087+1710G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233684 | ||||||
chr2:113233692
|
C | A | 6 | a0001c0001t0003g0195a0001c0001t0011g0024a0001c0001t0011g0025others(3): Show | 6 | HG01884.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1087+1702G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113233692 | ||||||
chr2:113234085
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0162 | 2 | NA18948.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1087+1309G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234085 | ||||||
chr2:113234086
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1087+1308C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234086 | ||||||
chr2:113234104
|
C | G | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1087+1290G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234104 | ||||||
chr2:113234123
|
T | C | 4 | a0001c0001t0018g0028a0001c0001t0023g0212a0001c0001t0032g0037others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+1271A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234123 | ||||||
chr2:113234216
|
T | A | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+1178A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234216 | ||||||
chr2:113234369
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1087+1025A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234369 | ||||||
chr2:113234393
|
A | G | 115 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(112): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1087+1001T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234393 | ||||||
chr2:113234581
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1087+813G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234581 | ||||||
chr2:113234624
|
G | A | 33 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1087+770C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234624 | ||||||
chr2:113234769
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0154 | 2 | HG01981.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1087+625G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234769 | ||||||
chr2:113234797
|
G | C | 160 | a0001c0001t0001g0190a0001c0001t0002g0004a0001c0001t0002g0012others(157): Show | 183 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1087+597C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234797 | ||||||
chr2:113234814
|
G | A | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1087+580C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234814 | ||||||
chr2:113234938
|
G | T | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+456C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113234938 | ||||||
chr2:113235047
|
T | C | 80 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(77): Show | 96 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1087+347A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113235047 | ||||||
chr2:113235071
|
A | C | 1 | a0001c0001t0037g0157 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1087+323T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113235071 | ||||||
chr2:113235183
|
C | T | 1 | a0001c0001t0012g0022 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1087+211G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113235183 | ||||||
chr2:113235223
|
TCC | T | 109 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(106): Show | 126 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1087+169_1087+170d others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113235223 | ||||||
chr2:113235390
|
G | A | 2 | a0001c0001t0018g0028a0001c0001t0032g0037 | 2 | HG01891.hp2 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.1087+4C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 9/11 | chr2 | 113235390 | ||||||
chr2:113235629
|
G | A | 1 | a0001c0001t0034g0245 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.899-47C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113235629 | ||||||
chr2:113235649
|
C | T | 3 | a0001c0003t0003g0126a0001c0003t0013g0026a0001c0003t0013g0027 | 3 | HG02257.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.899-67G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113235649 | ||||||
chr2:113235767
|
A | C | 108 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(105): Show | 125 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.899-185T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113235767 | ||||||
chr2:113235808
|
C | G | 110 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(107): Show | 127 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.899-226G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113235808 | ||||||
chr2:113235971
|
C | A | 1 | a0001c0001t0003g0016 | 2 | NA18967.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.899-389G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113235971 | ||||||
chr2:113235979
|
C | CGGCCCAC others(258): Show |
1 | a0001c0001t0002g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.899-398_899-397ins others(265): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113235979 | ||||||
chr2:113236006
|
A | ACCGGAGG others(171): Show |
1 | a0001c0001t0004g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.899-425_899-424ins others(178): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236006 | ||||||
chr2:113236007
|
C | T | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.899-425G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236007 | ||||||
chr2:113236015
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.899-433C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236015 | ||||||
chr2:113236031
|
G | C | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.899-449C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236031 | ||||||
chr2:113236068
|
C | G | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.899-486G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236068 | ||||||
chr2:113236081
|
G | A | 2 | a0001c0001t0004g0080a0001c0001t0032g0037 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.899-499C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236081 | ||||||
chr2:113236084
|
A | C | 2 | a0001c0001t0004g0080a0001c0001t0032g0037 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.899-502T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236084 | ||||||
chr2:113236085
|
G | C | 2 | a0001c0001t0004g0080a0001c0001t0032g0037 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.899-503C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236085 | ||||||
chr2:113236087
|
C | G | 2 | a0001c0001t0004g0080a0001c0001t0032g0037 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.899-505G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236087 | ||||||
chr2:113236097
|
C | CGGAGGCG others(81): Show |
1 | a0001c0001t0003g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.898+416_898+503dup others(88): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236097 | ||||||
chr2:113236097
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0032g0037 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.898+504G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236097 | ||||||
chr2:113236125
|
A | G | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+476T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236125 | ||||||
chr2:113236128
|
C | A | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+473G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236128 | ||||||
chr2:113236129
|
C | G | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+472G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236129 | ||||||
chr2:113236131
|
G | C | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+470C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236131 | ||||||
chr2:113236157
|
G | C | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+444C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236157 | ||||||
chr2:113236164
|
C | G | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+437G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236164 | ||||||
chr2:113236185
|
T | C | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+416A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236185 | ||||||
chr2:113236212
|
A | G | 29 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(26): Show | 35 | HG00323.hp2 HG01255.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.898+389T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236212 | ||||||
chr2:113236228
|
G | A | 2 | a0001c0001t0018g0028a0001c0001t0032g0037 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.898+373C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236228 | ||||||
chr2:113236230
|
CGGAGGCG others(81): Show |
C | 1 | a0001c0002t0003g0129 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.898+283_898+370del others(88): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236230 | ||||||
chr2:113236253
|
G | A | 2 | a0001c0001t0003g0125a0001c0001t0004g0080 | 2 | HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.898+348C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236253 | ||||||
chr2:113236253
|
G | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0032g0037 | 3 | HG01891.hp2 NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.898+348C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236253 | ||||||
chr2:113236274
|
CGGAGGCG others(125): Show |
C | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.898+195_898+326del | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236274 | ||||||
chr2:113236290
|
C | G | 53 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(50): Show | 63 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.898+311G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236290 | ||||||
chr2:113236290
|
CGGCCCAC others(81): Show |
C | 1 | a0001c0001t0001g0221 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.898+223_898+310del others(88): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236290 | ||||||
chr2:113236302
|
A | G | 2 | a0001c0001t0003g0125a0001c0001t0004g0080 | 2 | HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.898+299T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236302 | ||||||
chr2:113236305
|
C | A | 2 | a0001c0001t0003g0125a0001c0001t0004g0080 | 2 | HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.898+296G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236305 | ||||||
chr2:113236306
|
C | G | 2 | a0001c0001t0003g0125a0001c0001t0004g0080 | 2 | HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.898+295G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236306 | ||||||
chr2:113236308
|
G | C | 2 | a0001c0001t0003g0125a0001c0001t0004g0080 | 2 | HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.898+293C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236308 | ||||||
chr2:113236308
|
G | GGCCTAGG others(171): Show |
24 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(21): Show | 30 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.898+292_898+293ins others(178): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236308 | ||||||
chr2:113236318
|
T | C | 32 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0122others(29): Show | 38 | HG00323.hp2 HG00639.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.898+283A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236318 | ||||||
chr2:113236346
|
A | G | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+255T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236346 | ||||||
chr2:113236349
|
C | A | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+252G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236349 | ||||||
chr2:113236350
|
C | G | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+251G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236350 | ||||||
chr2:113236352
|
G | C | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898+249C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236352 | ||||||
chr2:113236362
|
CGGAGGCG others(37): Show |
C | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.898+195_898+238del others(44): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236362 | ||||||
chr2:113236378
|
G | C | 28 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(25): Show | 34 | HG00323.hp2 HG01255.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.898+223C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236378 | ||||||
chr2:113236378
|
G | GGGCCCAC others(170): Show |
1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.898+222_898+223ins others(177): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236378 | ||||||
chr2:113236378
|
G | GGGCCCAC others(171): Show |
1 | a0001c0001t0015g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.898+222_898+223ins others(178): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236378 | ||||||
chr2:113236378
|
G | GGGCCCAC others(215): Show |
1 | a0001c0001t0002g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.898+222_898+223ins others(222): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236378 | ||||||
chr2:113236378
|
G | GGGCCCAC others(215): Show |
72 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(69): Show | 83 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.898+222_898+223ins others(222): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236378 | ||||||
chr2:113236378
|
G | GGGCCCAC others(215): Show |
5 | a0001c0001t0004g0038a0001c0001t0004g0041a0001c0001t0004g0055others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+222_898+223ins others(222): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236378 | ||||||
chr2:113236406
|
T | C | 34 | a0001c0001t0001g0190a0001c0001t0002g0012a0001c0001t0002g0013others(31): Show | 37 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.898+195A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236406 | ||||||
chr2:113236498
|
G | C | 1 | a0001c0001t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.898+103C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236498 | ||||||
chr2:113236502
|
C | T | 76 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0091others(73): Show | 92 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.898+99G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236502 | ||||||
chr2:113236564
|
C | T | 2 | a0001c0001t0018g0028a0001c0001t0032g0037 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.898+37G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 8/11 | chr2 | 113236564 | ||||||
chr2:113236824
|
A | G | 1 | a0001c0001t0003g0016 | 2 | NA18967.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.778-103T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113236824 | ||||||
chr2:113236840
|
G | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(82): Show | 106 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.778-119C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113236840 | ||||||
chr2:113236884
|
G | A | 29 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0038others(26): Show | 30 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.778-163C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113236884 | ||||||
chr2:113236933
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(239): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.778-212T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113236933 | ||||||
chr2:113237018
|
C | T | 35 | a0001c0001t0001g0190a0001c0001t0002g0012a0001c0001t0002g0013others(32): Show | 38 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-297G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237018 | ||||||
chr2:113237069
|
C | G | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.778-348G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237069 | ||||||
chr2:113237169
|
T | C | 25 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0016others(22): Show | 31 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(28): Show |
intron_variant | MODIFIER | c.778-448A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237169 | ||||||
chr2:113237369
|
C | T | 5 | a0001c0001t0009g0031a0001c0001t0009g0119a0001c0001t0009g0120others(2): Show | 5 | HG02258.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-648G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237369 | ||||||
chr2:113237442
|
C | T | 1 | a0001c0001t0010g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.778-721G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237442 | ||||||
chr2:113237447
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.778-726C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237447 | ||||||
chr2:113237515
|
G | A | 5 | a0001c0001t0006g0077a0001c0001t0006g0078a0001c0001t0006g0079others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-794C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237515 | ||||||
chr2:113237697
|
C | T | 1 | a0001c0001t0036g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.778-976G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237697 | ||||||
chr2:113237719
|
T | C | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.778-998A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237719 | ||||||
chr2:113237825
|
C | G | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.778-1104G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237825 | ||||||
chr2:113237847
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.778-1126G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113237847 | ||||||
chr2:113238066
|
C | CT | 21 | a0001c0001t0001g0139a0001c0001t0001g0155a0001c0001t0001g0191others(18): Show | 21 | HG00735.hp2 HG02486.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-1346dupA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238066 | ||||||
chr2:113238066
|
CT | C | 28 | a0001c0001t0001g0127a0001c0001t0001g0206a0001c0001t0003g0008others(25): Show | 34 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-1346delA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238066 | ||||||
chr2:113238091
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 96 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.778-1370G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238091 | ||||||
chr2:113238216
|
C | T | 3 | a0001c0001t0009g0141a0001c0001t0026g0096a0001c0001t0028g0097 | 3 | HG01346.hp2 HG03239.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.778-1495G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238216 | ||||||
chr2:113238217
|
G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0019others(30): Show | 42 | HG00408.hp2 HG00673.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.778-1496C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238217 | ||||||
chr2:113238274
|
G | A | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.778-1553C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238274 | ||||||
chr2:113238357
|
G | A | 123 | a0001c0001t0001g0036a0001c0001t0001g0127a0001c0001t0001g0147others(120): Show | 140 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.778-1636C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238357 | ||||||
chr2:113238365
|
T | C | 60 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0158others(57): Show | 70 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.778-1644A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238365 | ||||||
chr2:113238441
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.778-1720T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238441 | ||||||
chr2:113238762
|
T | C | 96 | a0001c0001t0001g0036a0001c0001t0001g0147a0001c0001t0001g0155others(93): Show | 107 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.778-2041A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238762 | ||||||
chr2:113238863
|
C | T | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.778-2142G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238863 | ||||||
chr2:113238881
|
C | CAT | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.778-2161_778-2160i others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238881 | ||||||
chr2:113238978
|
CAA | C | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.778-2259_778-2258d others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238978 | ||||||
chr2:113238988
|
A | G | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.778-2267T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113238988 | ||||||
chr2:113239070
|
C | CT | 99 | a0001c0001t0001g0036a0001c0001t0001g0155a0001c0001t0001g0158others(96): Show | 112 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.778-2350dupA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239070 | ||||||
chr2:113239195
|
G | A | 27 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 33 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.777+2356C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239195 | ||||||
chr2:113239311
|
A | G | 124 | a0001c0001t0001g0036a0001c0001t0001g0127a0001c0001t0001g0147others(121): Show | 141 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.777+2240T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239311 | ||||||
chr2:113239371
|
C | A | 2 | a0001c0001t0006g0086a0001c0001t0019g0030 | 2 | HG01109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.777+2180G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239371 | ||||||
chr2:113239547
|
G | A | 7 | a0001c0001t0002g0214a0001c0001t0004g0040a0001c0001t0004g0052others(4): Show | 7 | NA18747.hp1 NA18960.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+2004C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239547 | ||||||
chr2:113239550
|
A | G | 1 | a0001c0001t0009g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.777+2001T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239550 | ||||||
chr2:113239717
|
T | C | 34 | a0001c0001t0001g0190a0001c0001t0002g0012a0001c0001t0002g0013others(31): Show | 37 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.777+1834A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239717 | ||||||
chr2:113239964
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0177a0001c0001t0001g0206 | 3 | NA18951.hp1 NA18984.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.777+1587C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113239964 | ||||||
chr2:113240101
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.777+1450A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240101 | ||||||
chr2:113240154
|
G | A | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.777+1397C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240154 | ||||||
chr2:113240268
|
G | A | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.777+1283C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240268 | ||||||
chr2:113240394
|
A | G | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+1157T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240394 | ||||||
chr2:113240408
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.777+1143T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240408 | ||||||
chr2:113240411
|
C | T | 1 | a0001c0001t0004g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.777+1140G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240411 | ||||||
chr2:113240458
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.777+1093C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240458 | ||||||
chr2:113240637
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.777+914C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240637 | ||||||
chr2:113240755
|
T | C | 32 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(29): Show | 33 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.777+796A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240755 | ||||||
chr2:113240829
|
GA | G | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.777+721delT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240829 | ||||||
chr2:113240898
|
CTG | C | 32 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(29): Show | 33 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.777+651_777+652del others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240898 | ||||||
chr2:113240958
|
T | G | 1 | a0001c0001t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.777+593A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113240958 | ||||||
chr2:113241124
|
C | T | 1 | a0001c0001t0029g0070 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.777+427G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113241124 | ||||||
chr2:113241446
|
T | C | 26 | a0001c0001t0001g0127a0001c0001t0002g0006a0001c0001t0002g0032others(23): Show | 34 | HG00323.hp2 HG01891.hp2 HG02071.hp1 others(31): Show |
intron_variant | MODIFIER | c.777+105A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 7/11 | chr2 | 113241446 | ||||||
chr2:113241804
|
C | G | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-78G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 6/11 | chr2 | 113241804 | ||||||
chr2:113241930
|
G | A | 1 | a0001c0003t0013g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.601+78C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 6/11 | chr2 | 113241930 | ||||||
chr2:113241957
|
G | C | 33 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.601+51C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 6/11 | chr2 | 113241957 | ||||||
chr2:113241971
|
C | T | 1 | a0001c0001t0017g0020 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.601+37G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 6/11 | chr2 | 113241971 | ||||||
chr2:113242136
|
G | A | 5 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.479-6C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242136 | ||||||
chr2:113242154
|
G | T | 1 | a0001c0001t0004g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.479-24C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242154 | ||||||
chr2:113242159
|
G | T | 80 | a0001c0001t0001g0036a0001c0001t0002g0076a0001c0001t0002g0088others(77): Show | 91 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.479-29C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242159 | ||||||
chr2:113242198
|
G | A | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.479-68C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242198 | ||||||
chr2:113242239
|
G | A | 1 | a0001c0001t0023g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.479-109C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242239 | ||||||
chr2:113242249
|
A | G | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.479-119T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242249 | ||||||
chr2:113242364
|
CTG | C | 32 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(29): Show | 33 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.479-236_479-235del others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242364 | ||||||
chr2:113242425
|
C | T | 5 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+265G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242425 | ||||||
chr2:113242530
|
T | C | 5 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+160A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242530 | ||||||
chr2:113242532
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.478+158C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242532 | ||||||
chr2:113242555
|
C | T | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.478+135G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242555 | ||||||
chr2:113242630
|
G | A | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.478+60C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242630 | ||||||
chr2:113242654
|
G | A | 1 | a0001c0001t0028g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.478+36C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 5/11 | chr2 | 113242654 | ||||||
chr2:113242881
|
C | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.390-103G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113242881 | ||||||
chr2:113243085
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.390-307C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243085 | ||||||
chr2:113243219
|
C | T | 1 | a0001c0001t0016g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-441G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243219 | ||||||
chr2:113243289
|
A | G | 145 | a0001c0001t0001g0036a0001c0001t0001g0127a0001c0001t0001g0244others(142): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.390-511T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243289 | ||||||
chr2:113243297
|
C | T | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.390-519G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243297 | ||||||
chr2:113243335
|
T | C | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.390-557A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243335 | ||||||
chr2:113243389
|
C | T | 32 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(29): Show | 33 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.390-611G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243389 | ||||||
chr2:113243397
|
CT | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(243): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.390-620delA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243397 | ||||||
chr2:113243482
|
C | A | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.390-704G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243482 | ||||||
chr2:113243615
|
C | T | 22 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(19): Show | 28 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.389+812G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243615 | ||||||
chr2:113243670
|
G | T | 33 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.389+757C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243670 | ||||||
chr2:113243786
|
A | G | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.389+641T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243786 | ||||||
chr2:113243861
|
C | A | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.389+566G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113243861 | ||||||
chr2:113244150
|
T | C | 5 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.389+277A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113244150 | ||||||
chr2:113244326
|
C | T | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.389+101G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113244326 | ||||||
chr2:113244344
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0004g0152others(1): Show | 4 | HG01106.hp1 HG02293.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+83T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 4/11 | chr2 | 113244344 | ||||||
chr2:113244754
|
G | T | 1 | a0001c0001t0004g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.192-130C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113244754 | ||||||
chr2:113244868
|
T | C | 36 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(33): Show | 39 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.192-244A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113244868 | ||||||
chr2:113244880
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192-256C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113244880 | ||||||
chr2:113244917
|
T | A | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.192-293A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113244917 | ||||||
chr2:113244933
|
G | C | 35 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(32): Show | 36 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.192-309C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113244933 | ||||||
chr2:113245045
|
G | GT | 56 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0001g0203others(53): Show | 69 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.192-422dupA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245045 | ||||||
chr2:113245045
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.192-421C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245045 | ||||||
chr2:113245055
|
T | TTTTG | 33 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.192-432_192-431ins others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245055 | ||||||
chr2:113245202
|
A | T | 103 | a0001c0001t0001g0036a0001c0001t0001g0127a0001c0001t0002g0076others(100): Show | 120 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.192-578T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245202 | ||||||
chr2:113245357
|
A | G | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.192-733T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245357 | ||||||
chr2:113245438
|
C | T | 1 | a0001c0001t0029g0070 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.192-814G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245438 | ||||||
chr2:113245465
|
C | T | 1 | a0001c0001t0005g0100 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.192-841G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245465 | ||||||
chr2:113245631
|
C | A | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.192-1007G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245631 | ||||||
chr2:113245660
|
G | A | 44 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0076others(41): Show | 54 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.192-1036C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245660 | ||||||
chr2:113245764
|
A | T | 4 | a0001c0001t0003g0140a0001c0001t0003g0181a0001c0001t0003g0182others(1): Show | 4 | NA18946.hp2 NA18950.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+990T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245764 | ||||||
chr2:113245888
|
G | T | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.191+866C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245888 | ||||||
chr2:113245902
|
A | G | 105 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0106others(102): Show | 122 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.191+852T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245902 | ||||||
chr2:113245955
|
A | T | 1 | a0001c0001t0003g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.191+799T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113245955 | ||||||
chr2:113246044
|
A | G | 149 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0106others(146): Show | 171 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.191+710T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246044 | ||||||
chr2:113246131
|
G | A | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.191+623C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246131 | ||||||
chr2:113246327
|
G | A | 103 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0106others(100): Show | 120 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.191+427C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246327 | ||||||
chr2:113246346
|
C | T | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.191+408G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246346 | ||||||
chr2:113246614
|
CTG | C | 6 | a0001c0001t0002g0012a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 7 | HG02280.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+138_191+139del others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246614 | ||||||
chr2:113246660
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.191+94C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246660 | ||||||
chr2:113246705
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.191+49C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 3/11 | chr2 | 113246705 | ||||||
chr2:113247188
|
C | T | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-269G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247188 | ||||||
chr2:113247195
|
C | T | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-276G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247195 | ||||||
chr2:113247322
|
TC | T | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-404delG | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247322 | ||||||
chr2:113247343
|
C | G | 1 | a0001c0001t0036g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-424G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247343 | ||||||
chr2:113247360
|
A | G | 21 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(18): Show | 27 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-441T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247360 | ||||||
chr2:113247417
|
A | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.26-498T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247417 | ||||||
chr2:113247523
|
TTCTC | T | 33 | a0001c0001t0001g0036a0001c0001t0002g0214a0001c0001t0003g0043others(30): Show | 34 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.26-608_26-605delGA others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247523 | ||||||
chr2:113247633
|
C | T | 1 | a0001c0001t0004g0046 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.26-714G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247633 | ||||||
chr2:113247640
|
T | C | 3 | a0001c0001t0002g0167a0001c0001t0008g0166a0001c0001t0008g0168 | 3 | NA18963.hp2 NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.26-721A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247640 | ||||||
chr2:113247756
|
T | C | 103 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0106others(100): Show | 120 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.26-837A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247756 | ||||||
chr2:113247848
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26-929T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113247848 | ||||||
chr2:113248002
|
G | A | 1 | a0002c0005t0001g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.26-1083C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113248002 | ||||||
chr2:113248133
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0004g0152 | 2 | HG01106.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.26-1214T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113248133 | ||||||
chr2:113248980
|
A | AAGGG | 44 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0076others(41): Show | 54 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.26-2065_26-2062dup others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113248980 | ||||||
chr2:113249123
|
A | G | 2 | a0001c0001t0006g0081a0001c0001t0006g0082 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.26-2204T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249123 | ||||||
chr2:113249132
|
C | T | 3 | a0001c0001t0014g0236a0001c0003t0013g0026a0001c0003t0013g0027 | 3 | HG02257.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.26-2213G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249132 | ||||||
chr2:113249257
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.26-2338G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249257 | ||||||
chr2:113249268
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.26-2349C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249268 | ||||||
chr2:113249589
|
T | A | 34 | a0001c0001t0001g0036a0001c0001t0001g0193a0001c0001t0002g0214others(31): Show | 35 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.26-2670A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249589 | ||||||
chr2:113249589
|
TA | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0230a0002c0005t0001g0201 | 3 | HG02897.hp2 HG03041.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.26-2671delT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249589 | ||||||
chr2:113249590
|
A | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0122others(1): Show | 7 | HG00639.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-2671T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249590 | ||||||
chr2:113249756
|
C | T | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-2837G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249756 | ||||||
chr2:113249891
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.26-2972C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249891 | ||||||
chr2:113249944
|
T | C | 78 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0106others(75): Show | 89 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.26-3025A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249944 | ||||||
chr2:113249997
|
G | T | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-3078C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113249997 | ||||||
chr2:113250037
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.26-3118C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250037 | ||||||
chr2:113250099
|
C | G | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.26-3180G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250099 | ||||||
chr2:113250266
|
C | CA | 73 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0227others(70): Show | 83 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.26-3348dupT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250266 | ||||||
chr2:113250266
|
C | CAA | 6 | a0001c0001t0002g0076a0001c0001t0008g0042a0001c0001t0008g0045others(3): Show | 6 | HG01109.hp1 HG02083.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-3349_26-3348dup others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250266 | ||||||
chr2:113250266
|
CA | C | 38 | a0001c0001t0001g0143a0001c0001t0001g0244a0001c0001t0002g0012others(35): Show | 41 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.26-3348delT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250266 | ||||||
chr2:113250376
|
G | A | 23 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0088others(20): Show | 32 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-3457C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250376 | ||||||
chr2:113250391
|
C | T | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-3472G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250391 | ||||||
chr2:113250593
|
T | G | 29 | a0001c0001t0001g0036a0001c0001t0003g0043a0001c0001t0003g0062others(26): Show | 30 | HG00673.hp2 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.26-3674A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250593 | ||||||
chr2:113250648
|
A | G | 1 | a0001c0003t0013g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-3729T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250648 | ||||||
chr2:113250808
|
C | A | 44 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0076others(41): Show | 54 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.26-3889G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250808 | ||||||
chr2:113250997
|
AG | A | 44 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0076others(41): Show | 54 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.26-4079delC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250997 | ||||||
chr2:113250998
|
G | A | 98 | a0001c0001t0001g0036a0001c0001t0001g0127a0001c0001t0001g0244others(95): Show | 110 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.26-4079C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113250998 | ||||||
chr2:113251077
|
A | T | 6 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4158T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113251077 | ||||||
chr2:113251548
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0016a0001c0001t0003g0138 | 6 | NA18967.hp1 NA18980.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-4629C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113251548 | ||||||
chr2:113251580
|
G | A | 2 | a0001c0003t0013g0026a0001c0003t0013g0027 | 2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.26-4661C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113251580 | ||||||
chr2:113251701
|
T | C | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26-4782A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113251701 | ||||||
chr2:113251752
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(98): Show | 122 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.26-4833A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113251752 | ||||||
chr2:113251835
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.26-4916G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113251835 | ||||||
chr2:113252367
|
A | G | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-5448T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113252367 | ||||||
chr2:113252442
|
C | T | 1 | a0001c0004t0007g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.26-5523G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113252442 | ||||||
chr2:113252471
|
C | T | 38 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0088others(35): Show | 48 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.26-5552G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113252471 | ||||||
chr2:113252584
|
GGAAAGC | G | 56 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0127others(53): Show | 63 | HG00140.hp1 HG00323.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-5671_26-5666del others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113252584 | ||||||
chr2:113252735
|
C | T | 6 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-5816G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113252735 | ||||||
chr2:113253016
|
T | C | 32 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0003g0043others(29): Show | 33 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-6097A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253016 | ||||||
chr2:113253155
|
T | G | 2 | a0001c0001t0003g0043a0001c0001t0003g0062 | 2 | NA19001.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.26-6236A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253155 | ||||||
chr2:113253190
|
T | C | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-6271A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253190 | ||||||
chr2:113253192
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.26-6273G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253192 | ||||||
chr2:113253214
|
C | T | 49 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0127others(46): Show | 56 | HG00140.hp1 HG00323.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-6295G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253214 | ||||||
chr2:113253300
|
T | C | 2 | a0001c0001t0004g0047a0001c0001t0004g0058 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.26-6381A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253300 | ||||||
chr2:113253485
|
A | G | 14 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(11): Show | 14 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.26-6566T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253485 | ||||||
chr2:113253518
|
C | T | 6 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0073others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-6599G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253518 | ||||||
chr2:113253690
|
T | G | 1 | a0003c0010t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-6771A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253690 | ||||||
chr2:113253738
|
A | G | 1 | a0003c0010t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-6819T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253738 | ||||||
chr2:113253752
|
T | C | 13 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(10): Show | 13 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-6833A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253752 | ||||||
chr2:113253854
|
G | A | 13 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(10): Show | 13 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-6935C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253854 | ||||||
chr2:113253970
|
A | G | 1 | a0001c0001t0003g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.26-7051T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113253970 | ||||||
chr2:113254133
|
C | T | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-7214G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254133 | ||||||
chr2:113254175
|
C | T | 75 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(72): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.26-7256G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254175 | ||||||
chr2:113254190
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.26-7271G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254190 | ||||||
chr2:113254274
|
A | G | 14 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(11): Show | 14 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.26-7355T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254274 | ||||||
chr2:113254337
|
A | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 121 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.26-7418T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254337 | ||||||
chr2:113254406
|
C | T | 13 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(10): Show | 13 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-7487G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254406 | ||||||
chr2:113254470
|
G | C | 38 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0088others(35): Show | 48 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.26-7551C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254470 | ||||||
chr2:113254519
|
A | G | 101 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0127others(98): Show | 122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.26-7600T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254519 | ||||||
chr2:113254766
|
A | G | 4 | a0001c0001t0003g0140a0001c0001t0003g0181a0001c0001t0003g0182others(1): Show | 4 | NA18946.hp2 NA18950.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-7847T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254766 | ||||||
chr2:113254773
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02080.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.26-7854G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254773 | ||||||
chr2:113254816
|
A | G | 13 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(10): Show | 13 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-7897T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254816 | ||||||
chr2:113254846
|
A | C | 13 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(10): Show | 13 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-7927T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254846 | ||||||
chr2:113254847
|
G | A | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-7928C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254847 | ||||||
chr2:113254965
|
G | A | 147 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(144): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.26-8046C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113254965 | ||||||
chr2:113255032
|
A | G | 1 | a0001c0001t0015g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.26-8113T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255032 | ||||||
chr2:113255089
|
A | AAAAGAAG others(63): Show |
1 | a0001c0001t0003g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.26-8171_26-8170ins others(70): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255089 | ||||||
chr2:113255093
|
AGAAG | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(5): Show | 10 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-8178_26-8175del others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255093 | ||||||
chr2:113255094
|
G | A | 1 | a0001c0001t0003g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.26-8175C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255094 | ||||||
chr2:113255094
|
G | GAAGGAAG others(64): Show |
43 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0127others(40): Show | 50 | HG00140.hp1 HG00323.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.26-8176_26-8175ins others(71): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255094 | ||||||
chr2:113255130
|
A | AAGGAAGG others(60): Show |
6 | a0001c0001t0008g0042a0001c0001t0008g0045a0001c0001t0008g0057others(3): Show | 6 | HG01884.hp1 HG02083.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-8212_26-8211ins others(67): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255130 | ||||||
chr2:113255146
|
AAAG | A | 6 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8230_26-8228del others(3): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255146 | ||||||
chr2:113255209
|
AAGGAGGG others(5): Show |
A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(93): Show | 117 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.26-8302_26-8291del others(12): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255209 | ||||||
chr2:113255218
|
G | C | 7 | a0001c0001t0004g0011a0001c0001t0004g0038a0001c0001t0004g0041others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-8299C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255218 | ||||||
chr2:113255230
|
G | GGGGAGGA others(4): Show |
13 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0128others(10): Show | 16 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-8322_26-8312dup others(11): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255230 | ||||||
chr2:113255230
|
GGGGAGGA others(16): Show |
G | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.26-8334_26-8312del others(23): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255230 | ||||||
chr2:113255241
|
AG | A | 16 | a0001c0001t0001g0197a0001c0001t0003g0009a0001c0001t0003g0016others(13): Show | 19 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-8323delC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255241 | ||||||
chr2:113255241
|
AGGGGAGG others(17): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.26-8346_26-8323del others(24): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255241 | ||||||
chr2:113255241
|
AGGGGAGG others(29): Show |
A | 1 | a0001c0009t0014g0223 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.26-8358_26-8323del others(36): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255241 | ||||||
chr2:113255242
|
G | GGGAGGAG others(37): Show |
5 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-8324_26-8323ins others(44): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255242 | ||||||
chr2:113255242
|
GGGGAGGA others(4): Show |
G | 42 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0004others(39): Show | 55 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.26-8334_26-8324del others(11): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255242 | ||||||
chr2:113255253
|
A | AG | 21 | a0001c0001t0001g0127a0001c0001t0001g0197a0001c0001t0003g0008others(18): Show | 27 | HG00323.hp2 HG01884.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-8335dupC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255253 | ||||||
chr2:113255253
|
A | AGGGAGGA others(5): Show |
1 | a0001c0001t0004g0047 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.26-8346_26-8335dup others(12): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255253 | ||||||
chr2:113255253
|
A | AGGGGAGG others(6): Show |
1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.26-8335_26-8334ins others(13): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255253 | ||||||
chr2:113255253
|
AGGGAGGA others(17): Show |
A | 45 | a0001c0001t0001g0244a0001c0001t0002g0006a0001c0001t0002g0012others(42): Show | 50 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.26-8358_26-8335del others(24): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255253 | ||||||
chr2:113255254
|
GGGAGGAG others(3): Show |
G | 1 | a0001c0001t0008g0168 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.26-8345_26-8336del others(10): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255254 | ||||||
chr2:113255264
|
AGGGGAGG others(17): Show |
A | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-8369_26-8346del others(24): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255264 | ||||||
chr2:113255265
|
G | GGGA | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-8347_26-8346ins others(3): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255265 | ||||||
chr2:113255276
|
AG | A | 53 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0127others(50): Show | 66 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.26-8358delC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255276 | ||||||
chr2:113255277
|
G | A | 1 | a0001c0001t0008g0168 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.26-8358C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255277 | ||||||
chr2:113255277
|
G | GGGAGGAG others(37): Show |
7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-8359_26-8358ins others(44): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255277 | ||||||
chr2:113255277
|
G | GGGGAGGA others(4): Show |
4 | a0001c0001t0003g0009a0001c0001t0003g0016a0001c0001t0003g0138others(1): Show | 7 | HG01884.hp1 NA18967.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-8369_26-8359dup others(11): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255277 | ||||||
chr2:113255277
|
G | GGGGAGGA others(51): Show |
1 | a0001c0001t0004g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26-8359_26-8358ins others(58): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255277 | ||||||
chr2:113255277
|
G | GGGGAGGA others(16): Show |
28 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0003g0043others(25): Show | 29 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.26-8359_26-8358ins others(23): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255277 | ||||||
chr2:113255280
|
G | A | 1 | a0001c0001t0006g0079 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.26-8361C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255280 | ||||||
chr2:113255288
|
A | AG | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-8370dupC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255288 | ||||||
chr2:113255288
|
AGGGAGGA others(5): Show |
A | 1 | a0001c0001t0001g0216 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.26-8381_26-8370del others(12): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255288 | ||||||
chr2:113255305
|
G | C | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-8386C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255305 | ||||||
chr2:113255305
|
G | GGAGGGAG others(62): Show |
5 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-8387_26-8386ins others(69): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255305 | ||||||
chr2:113255305
|
G | GGAGGGAG others(97): Show |
1 | a0001c0001t0006g0079 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.26-8387_26-8386ins others(104): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255305 | ||||||
chr2:113255351
|
A | T | 84 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(81): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.26-8432T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255351 | ||||||
chr2:113255452
|
A | C | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(5): Show | 10 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-8533T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255452 | ||||||
chr2:113255535
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.26-8616C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255535 | ||||||
chr2:113255692
|
G | C | 38 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0002g0088others(35): Show | 48 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.26-8773C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255692 | ||||||
chr2:113255887
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.26-8968G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255887 | ||||||
chr2:113255891
|
T | C | 97 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(94): Show | 112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.26-8972A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255891 | ||||||
chr2:113255965
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-9046G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255965 | ||||||
chr2:113255994
|
T | TA | 111 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(108): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.26-9076dupT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255994 | ||||||
chr2:113255994
|
T | TAAA | 7 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(4): Show | 9 | HG02258.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-9078_26-9076dup others(3): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255994 | ||||||
chr2:113255995
|
A | T | 2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.26-9076T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113255995 | ||||||
chr2:113256067
|
G | A | 1 | a0001c0001t0002g0013 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.26-9148C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256067 | ||||||
chr2:113256195
|
G | A | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-9276C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256195 | ||||||
chr2:113256316
|
T | C | 1 | a0001c0001t0004g0056 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.26-9397A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256316 | ||||||
chr2:113256346
|
G | A | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26-9427C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256346 | ||||||
chr2:113256457
|
A | G | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26-9538T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256457 | ||||||
chr2:113256570
|
C | CTA | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(5): Show | 10 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-9653_26-9652dup others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256570 | ||||||
chr2:113256573
|
T | TAG | 74 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(71): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.26-9655_26-9654ins others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256573 | ||||||
chr2:113256606
|
ATG | A | 54 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0127others(51): Show | 61 | HG00140.hp1 HG00323.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.26-9689_26-9688del others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256606 | ||||||
chr2:113256614
|
GTGTA | G | 83 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(80): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.26-9699_26-9696del others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256614 | ||||||
chr2:113256616
|
G | A | 9 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(6): Show | 11 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-9697C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256616 | ||||||
chr2:113256626
|
ATATATGT others(3): Show |
A | 7 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(4): Show | 9 | HG02258.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-9717_26-9708del others(10): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256626 | ||||||
chr2:113256628
|
A | G | 1 | a0001c0001t0004g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26-9709T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256628 | ||||||
chr2:113256630
|
A | G | 32 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0003g0043others(29): Show | 33 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-9711T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256630 | ||||||
chr2:113256630
|
ATG | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(91): Show | 114 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.26-9713_26-9712del others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256630 | ||||||
chr2:113256632
|
G | A | 1 | a0001c0001t0007g0169 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.26-9713C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256632 | ||||||
chr2:113256650
|
GTGTGTA | G | 73 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(70): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.26-9737_26-9732del others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256650 | ||||||
chr2:113256652
|
GTGTATA | G | 14 | a0001c0001t0002g0064a0001c0001t0002g0076a0001c0001t0006g0077others(11): Show | 14 | HG01109.hp1 HG02109.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.26-9739_26-9734del others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256652 | ||||||
chr2:113256654
|
G | A | 11 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0003g0128others(8): Show | 12 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-9735C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256654 | ||||||
chr2:113256654
|
GTA | G | 5 | a0001c0001t0001g0149a0001c0001t0002g0176a0001c0001t0010g0018others(2): Show | 6 | HG00642.hp1 HG02071.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-9737_26-9736del others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256654 | ||||||
chr2:113256656
|
A | G | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.26-9737T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256656 | ||||||
chr2:113256775
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.26-9856T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256775 | ||||||
chr2:113256815
|
T | C | 7 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(4): Show | 9 | HG02258.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-9896A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256815 | ||||||
chr2:113256842
|
C | A | 1 | a0001c0009t0014g0223 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.26-9923G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113256842 | ||||||
chr2:113257065
|
G | A | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-10146C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257065 | ||||||
chr2:113257124
|
A | C | 147 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(144): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.26-10205T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257124 | ||||||
chr2:113257176
|
C | G | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-10257G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257176 | ||||||
chr2:113257233
|
T | C | 1 | a0001c0001t0030g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.26-10314A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257233 | ||||||
chr2:113257268
|
G | T | 6 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-10349C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257268 | ||||||
chr2:113257359
|
C | G | 4 | a0001c0001t0008g0042a0001c0001t0008g0045a0001c0001t0008g0057others(1): Show | 4 | HG02083.hp1 NA18994.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-10440G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257359 | ||||||
chr2:113257371
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.26-10452T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257371 | ||||||
chr2:113257606
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.26-10687A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257606 | ||||||
chr2:113257634
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.26-10715C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257634 | ||||||
chr2:113257731
|
A | C | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-10812T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257731 | ||||||
chr2:113257861
|
T | C | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-10942A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257861 | ||||||
chr2:113257887
|
A | G | 6 | a0001c0001t0002g0076a0001c0001t0006g0077a0001c0001t0006g0078others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-10968T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113257887 | ||||||
chr2:113258115
|
C | G | 84 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(81): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.26-11196G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258115 | ||||||
chr2:113258185
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-11266C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258185 | ||||||
chr2:113258418
|
C | T | 1 | a0001c0001t0029g0070 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.26-11499G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258418 | ||||||
chr2:113258494
|
G | A | 85 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0244others(82): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.26-11575C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258494 | ||||||
chr2:113258581
|
G | C | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-11662C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258581 | ||||||
chr2:113258629
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.26-11710T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258629 | ||||||
chr2:113258731
|
A | G | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26-11812T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258731 | ||||||
chr2:113258765
|
C | G | 4 | a0001c0001t0003g0140a0001c0001t0003g0181a0001c0001t0003g0182others(1): Show | 4 | NA18946.hp2 NA18950.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-11846G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258765 | ||||||
chr2:113258824
|
C | T | 11 | a0001c0001t0002g0014a0001c0001t0002g0034a0001c0001t0002g0089others(8): Show | 12 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-11905G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258824 | ||||||
chr2:113258925
|
T | A | 1 | a0001c0001t0004g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.26-12006A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113258925 | ||||||
chr2:113259039
|
T | A | 2 | a0001c0001t0006g0081a0001c0001t0006g0082 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.26-12120A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259039 | ||||||
chr2:113259063
|
A | G | 4 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-12144T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259063 | ||||||
chr2:113259083
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-12164C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259083 | ||||||
chr2:113259105
|
G | A | 1 | a0001c0001t0008g0057 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.26-12186C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259105 | ||||||
chr2:113259260
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.26-12341C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259260 | ||||||
chr2:113259315
|
C | T | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26-12396G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259315 | ||||||
chr2:113259428
|
C | T | 18 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 24 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-12509G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259428 | ||||||
chr2:113259452
|
A | G | 147 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(144): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.26-12533T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259452 | ||||||
chr2:113259578
|
G | A | 8 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0122others(5): Show | 11 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-12659C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259578 | ||||||
chr2:113259657
|
C | G | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-12738G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259657 | ||||||
chr2:113259705
|
C | CATTA | 153 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(150): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.26-12790_26-12787d others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259705 | ||||||
chr2:113259746
|
A | G | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-12827T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259746 | ||||||
chr2:113259945
|
G | A | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-13026C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259945 | ||||||
chr2:113259953
|
G | A | 1 | a0001c0001t0016g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-13034C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113259953 | ||||||
chr2:113260030
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.26-13111C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260030 | ||||||
chr2:113260047
|
G | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0122others(4): Show | 10 | HG00639.hp2 HG02258.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-13128C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260047 | ||||||
chr2:113260050
|
T | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0122others(8): Show | 14 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.26-13131A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260050 | ||||||
chr2:113260075
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.26-13156T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260075 | ||||||
chr2:113260139
|
G | A | 7 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-13220C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260139 | ||||||
chr2:113260236
|
A | G | 1 | a0001c0001t0003g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.26-13317T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260236 | ||||||
chr2:113260298
|
T | C | 86 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0114others(83): Show | 101 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.26-13379A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260298 | ||||||
chr2:113260360
|
T | C | 98 | a0001c0001t0001g0010a0001c0001t0001g0061a0001c0001t0001g0106others(95): Show | 115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.26-13441A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260360 | ||||||
chr2:113260361
|
G | A | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-13442C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260361 | ||||||
chr2:113260488
|
CAG | C | 44 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(41): Show | 47 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-13571_26-13570d others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260488 | ||||||
chr2:113260516
|
G | A | 1 | a0001c0001t0004g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.26-13597C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260516 | ||||||
chr2:113260701
|
C | T | 7 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG01884.hp1 HG02080.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-13782G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260701 | ||||||
chr2:113260743
|
C | T | 144 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(141): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.26-13824G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260743 | ||||||
chr2:113260812
|
C | T | 2 | a0001c0001t0014g0236a0001c0001t0036g0117 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.26-13893G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260812 | ||||||
chr2:113260830
|
T | G | 40 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0106others(37): Show | 43 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.26-13911A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260830 | ||||||
chr2:113260878
|
T | TTG | 9 | a0001c0001t0001g0190a0001c0001t0002g0006a0001c0001t0002g0032others(6): Show | 11 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-13961_26-13960d others(4): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260878 | ||||||
chr2:113260878
|
T | TTGTG | 9 | a0001c0001t0002g0013a0001c0001t0002g0067a0001c0001t0011g0024others(6): Show | 10 | HG02109.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-13963_26-13960d others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260878 | ||||||
chr2:113260878
|
T | TTGTGTGT others(1): Show |
25 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0063others(22): Show | 26 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-13967_26-13960d others(10): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260878 | ||||||
chr2:113260878
|
T | TTGTGTGT others(3): Show |
6 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0073others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-13969_26-13960d others(12): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260878 | ||||||
chr2:113260900
|
A | G | 44 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(41): Show | 46 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.26-13981T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113260900 | ||||||
chr2:113261013
|
C | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(38): Show | 44 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.26-14094G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261013 | ||||||
chr2:113261078
|
T | C | 16 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(13): Show | 22 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.26-14159A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261078 | ||||||
chr2:113261249
|
G | A | 41 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 43 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.26-14330C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261249 | ||||||
chr2:113261422
|
G | A | 2 | a0001c0003t0013g0026a0001c0003t0013g0027 | 2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.26-14503C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261422 | ||||||
chr2:113261514
|
A | G | 41 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(38): Show | 44 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.26-14595T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261514 | ||||||
chr2:113261552
|
G | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(38): Show | 44 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.26-14633C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261552 | ||||||
chr2:113261602
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.26-14683C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261602 | ||||||
chr2:113261603
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.26-14684T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261603 | ||||||
chr2:113261604
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.26-14685C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261604 | ||||||
chr2:113261605
|
G | A | 49 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0114others(46): Show | 62 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.26-14686C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261605 | ||||||
chr2:113261610
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.26-14691A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261610 | ||||||
chr2:113261613
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.26-14694T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261613 | ||||||
chr2:113261684
|
G | A | 2 | a0001c0001t0002g0113a0001c0001t0002g0115 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.26-14765C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261684 | ||||||
chr2:113261773
|
G | A | 41 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 43 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.26-14854C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261773 | ||||||
chr2:113261778
|
C | T | 1 | a0001c0001t0001g0005 | 4 | HG01975.hp1 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-14859G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261778 | ||||||
chr2:113261801
|
T | G | 83 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0244others(80): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.26-14882A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261801 | ||||||
chr2:113261822
|
G | GT | 11 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0188others(8): Show | 11 | HG00673.hp1 HG01109.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-14904dupA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261822 | ||||||
chr2:113261822
|
GT | G | 18 | a0001c0001t0001g0127a0001c0001t0001g0220a0001c0001t0003g0008others(15): Show | 24 | HG00323.hp2 HG02015.hp1 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-14904delA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261822 | ||||||
chr2:113261882
|
G | A | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-14963C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113261882 | ||||||
chr2:113262207
|
GA | G | 16 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(13): Show | 22 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.26-15289delT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262207 | ||||||
chr2:113262374
|
G | A | 41 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(38): Show | 44 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.26-15455C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262374 | ||||||
chr2:113262377
|
A | T | 16 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(13): Show | 22 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.26-15458T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262377 | ||||||
chr2:113262385
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.26-15466G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262385 | ||||||
chr2:113262400
|
T | A | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.26-15481A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262400 | ||||||
chr2:113262416
|
G | A | 38 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0114others(35): Show | 48 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.26-15497C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262416 | ||||||
chr2:113262474
|
G | C | 50 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0114others(47): Show | 63 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.26-15555C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262474 | ||||||
chr2:113262543
|
G | C | 83 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0244others(80): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.26-15624C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262543 | ||||||
chr2:113262802
|
C | T | 42 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 44 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+15568G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262802 | ||||||
chr2:113262969
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.25+15401T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113262969 | ||||||
chr2:113263061
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA19056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.25+15309G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263061 | ||||||
chr2:113263251
|
G | T | 149 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(146): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.25+15119C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263251 | ||||||
chr2:113263271
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 126 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.25+15099A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263271 | ||||||
chr2:113263275
|
C | T | 2 | a0001c0001t0006g0086a0001c0001t0019g0030 | 2 | HG01109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.25+15095G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263275 | ||||||
chr2:113263331
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.25+15039A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263331 | ||||||
chr2:113263334
|
C | G | 41 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 43 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+15036G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263334 | ||||||
chr2:113263334
|
C | T | 47 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0114others(44): Show | 60 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.25+15036G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263334 | ||||||
chr2:113263541
|
G | A | 41 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 43 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+14829C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263541 | ||||||
chr2:113263769
|
G | A | 1 | a0001c0001t0007g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25+14601C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263769 | ||||||
chr2:113263833
|
G | A | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25+14537C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263833 | ||||||
chr2:113263897
|
C | T | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+14473G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113263897 | ||||||
chr2:113264055
|
T | G | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.25+14315A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264055 | ||||||
chr2:113264144
|
G | T | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25+14226C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264144 | ||||||
chr2:113264351
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.25+14019C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264351 | ||||||
chr2:113264588
|
T | G | 1 | a0001c0001t0017g0020 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.25+13782A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264588 | ||||||
chr2:113264589
|
T | G | 1 | a0001c0001t0017g0020 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.25+13781A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264589 | ||||||
chr2:113264609
|
G | C | 1 | a0001c0001t0003g0138 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.25+13761C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264609 | ||||||
chr2:113264625
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.25+13745C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264625 | ||||||
chr2:113264686
|
T | C | 1 | a0001c0001t0007g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25+13684A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264686 | ||||||
chr2:113264921
|
G | A | 2 | a0001c0001t0010g0018a0001c0001t0010g0179 | 3 | HG02738.hp2 HG04199.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.25+13449C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264921 | ||||||
chr2:113264992
|
C | A | 26 | a0001c0001t0001g0244a0001c0001t0002g0013a0001c0001t0002g0067others(23): Show | 27 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+13378G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113264992 | ||||||
chr2:113265081
|
T | C | 149 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(146): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.25+13289A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265081 | ||||||
chr2:113265102
|
C | G | 1 | a0001c0001t0004g0041 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.25+13268G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265102 | ||||||
chr2:113265195
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.25+13175C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265195 | ||||||
chr2:113265279
|
G | A | 41 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(38): Show | 44 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.25+13091C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265279 | ||||||
chr2:113265370
|
G | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(1): Show | 6 | HG02622.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+13000C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265370 | ||||||
chr2:113265502
|
C | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(38): Show | 44 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.25+12868G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265502 | ||||||
chr2:113265640
|
G | A | 83 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0244others(80): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.25+12730C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265640 | ||||||
chr2:113265666
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.25+12704T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113265666 | ||||||
chr2:113266063
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25+12307T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266063 | ||||||
chr2:113266149
|
A | G | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25+12221T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266149 | ||||||
chr2:113266203
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.25+12167T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266203 | ||||||
chr2:113266306
|
G | A | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+12064C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266306 | ||||||
chr2:113266731
|
C | A | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.25+11639G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266731 | ||||||
chr2:113266760
|
G | T | 2 | a0001c0003t0013g0026a0001c0003t0013g0027 | 2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.25+11610C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266760 | ||||||
chr2:113266843
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.25+11527A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266843 | ||||||
chr2:113266928
|
T | C | 84 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0222others(81): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.25+11442A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113266928 | ||||||
chr2:113267017
|
T | G | 9 | a0001c0001t0002g0091a0001c0001t0002g0107a0001c0001t0002g0108others(6): Show | 9 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+11353A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267017 | ||||||
chr2:113267269
|
C | T | 41 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 43 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+11101G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267269 | ||||||
chr2:113267520
|
C | G | 1 | a0001c0001t0036g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25+10850G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267520 | ||||||
chr2:113267531
|
G | A | 1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.25+10839C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267531 | ||||||
chr2:113267566
|
T | G | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+10804A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267566 | ||||||
chr2:113267678
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.25+10692G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267678 | ||||||
chr2:113267721
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.25+10649A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267721 | ||||||
chr2:113267795
|
A | G | 38 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0114others(35): Show | 48 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.25+10575T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267795 | ||||||
chr2:113267825
|
A | T | 99 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0127others(96): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.25+10545T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267825 | ||||||
chr2:113267874
|
G | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0188a0001c0001t0001g0189 | 4 | NA18941.hp1 NA18994.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+10496C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267874 | ||||||
chr2:113267995
|
G | C | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.25+10375C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113267995 | ||||||
chr2:113268084
|
C | G | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+10286G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113268084 | ||||||
chr2:113268309
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0018g0028 | 2 | HG03130.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.25+10061T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113268309 | ||||||
chr2:113268591
|
C | T | 1 | a0001c0001t0009g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.25+9779G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113268591 | ||||||
chr2:113268763
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+9607G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113268763 | ||||||
chr2:113268806
|
C | T | 34 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0002g0006others(31): Show | 37 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.25+9564G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113268806 | ||||||
chr2:113269238
|
C | A | 4 | a0001c0001t0014g0236a0001c0001t0036g0117a0001c0003t0013g0026others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+9132G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113269238 | ||||||
chr2:113269305
|
G | C | 148 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(145): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.25+9065C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113269305 | ||||||
chr2:113269358
|
G | C | 1 | a0001c0001t0021g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25+9012C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113269358 | ||||||
chr2:113269476
|
C | T | 1 | a0001c0001t0003g0090 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.25+8894G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113269476 | ||||||
chr2:113269828
|
G | A | 100 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(97): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.25+8542C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113269828 | ||||||
chr2:113269882
|
C | T | 100 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(97): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.25+8488G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113269882 | ||||||
chr2:113270374
|
G | A | 147 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(144): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.25+7996C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270374 | ||||||
chr2:113270583
|
G | C | 3 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0022g0124 | 4 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+7787C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270583 | ||||||
chr2:113270592
|
G | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 127 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.25+7778C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270592 | ||||||
chr2:113270691
|
A | T | 1 | a0001c0001t0004g0142 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.25+7679T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270691 | ||||||
chr2:113270855
|
GA | G | 100 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(97): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.25+7514delT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270855 | ||||||
chr2:113270906
|
C | T | 17 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(14): Show | 23 | HG00323.hp2 HG01109.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+7464G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270906 | ||||||
chr2:113270931
|
G | A | 1 | a0001c0001t0006g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.25+7439C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270931 | ||||||
chr2:113270989
|
A | C | 1 | a0001c0001t0004g0040 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.25+7381T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113270989 | ||||||
chr2:113271067
|
G | A | 1 | a0001c0001t0003g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.25+7303C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271067 | ||||||
chr2:113271096
|
T | C | 17 | a0001c0001t0001g0127a0001c0001t0003g0008a0001c0001t0003g0009others(14): Show | 23 | HG00323.hp2 HG01109.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+7274A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271096 | ||||||
chr2:113271143
|
C | A | 1 | a0001c0001t0003g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.25+7227G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271143 | ||||||
chr2:113271143
|
C | T | 41 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(38): Show | 43 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+7227G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271143 | ||||||
chr2:113271444
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0003g0140a0001c0001t0003g0181others(2): Show | 5 | NA18950.hp1 NA18994.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+6926C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271444 | ||||||
chr2:113271639
|
C | T | 1 | a0001c0001t0004g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.25+6731G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271639 | ||||||
chr2:113271663
|
G | T | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.25+6707C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271663 | ||||||
chr2:113271701
|
G | A | 1 | a0001c0001t0024g0250 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25+6669C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271701 | ||||||
chr2:113271747
|
A | T | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.25+6623T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271747 | ||||||
chr2:113271832
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | NA18997.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.25+6538C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113271832 | ||||||
chr2:113272066
|
A | G | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.25+6304T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272066 | ||||||
chr2:113272125
|
CACAGAA | C | 58 | a0001c0001t0001g0127a0001c0001t0001g0244a0001c0001t0002g0012others(55): Show | 66 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.25+6239_25+6244del others(6): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272125 | ||||||
chr2:113272190
|
G | A | 7 | a0001c0001t0002g0076a0001c0001t0004g0080a0001c0001t0006g0077others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+6180C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272190 | ||||||
chr2:113272192
|
C | T | 35 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(32): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.25+6178G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272192 | ||||||
chr2:113272308
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.25+6062A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272308 | ||||||
chr2:113272408
|
C | G | 1 | a0001c0003t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+5962G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272408 | ||||||
chr2:113272553
|
C | T | 2 | a0001c0001t0003g0130a0001c0001t0003g0185 | 2 | HG02074.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.25+5817G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272553 | ||||||
chr2:113272668
|
A | T | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.25+5702T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272668 | ||||||
chr2:113272838
|
T | C | 17 | a0001c0001t0001g0127a0001c0001t0002g0131a0001c0001t0003g0008others(14): Show | 23 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+5532A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113272838 | ||||||
chr2:113273023
|
G | A | 40 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(37): Show | 42 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.25+5347C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273023 | ||||||
chr2:113273046
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.25+5324G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273046 | ||||||
chr2:113273348
|
G | A | 18 | a0001c0001t0001g0127a0001c0001t0002g0131a0001c0001t0003g0008others(15): Show | 24 | HG00323.hp2 HG01109.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+5022C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273348 | ||||||
chr2:113273358
|
G | A | 2 | a0001c0001t0014g0236a0001c0001t0036g0117 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.25+5012C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273358 | ||||||
chr2:113273433
|
T | C | 2 | a0001c0001t0014g0236a0001c0001t0036g0117 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.25+4937A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273433 | ||||||
chr2:113273464
|
T | TTC | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.25+4905_25+4906ins others(2): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273464 | ||||||
chr2:113273767
|
A | AT | 38 | a0001c0001t0001g0244a0001c0001t0002g0012a0001c0001t0002g0013others(35): Show | 40 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.25+4602dupA | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273767 | ||||||
chr2:113273811
|
G | A | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.25+4559C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273811 | ||||||
chr2:113273930
|
A | G | 2 | a0001c0001t0003g0128a0001c0002t0003g0129 | 2 | NA18956.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.25+4440T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273930 | ||||||
chr2:113273960
|
A | G | 7 | a0001c0001t0002g0076a0001c0001t0004g0080a0001c0001t0006g0077others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+4410T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113273960 | ||||||
chr2:113274021
|
C | CGTGCGTG others(3): Show |
1 | a0001c0001t0018g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.25+4339_25+4348dup others(10): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274021 | ||||||
chr2:113274074
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.25+4296G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274074 | ||||||
chr2:113274100
|
C | T | 1 | a0001c0001t0036g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25+4270G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274100 | ||||||
chr2:113274211
|
G | A | 5 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(2): Show | 5 | HG02258.hp1 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+4159C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274211 | ||||||
chr2:113274239
|
C | A | 1 | a0001c0001t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.25+4131G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274239 | ||||||
chr2:113274244
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.25+4126C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274244 | ||||||
chr2:113274621
|
A | T | 2 | a0001c0003t0013g0026a0001c0003t0013g0027 | 2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.25+3749T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274621 | ||||||
chr2:113274626
|
A | G | 3 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0022g0124 | 4 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+3744T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274626 | ||||||
chr2:113274694
|
A | C | 1 | a0001c0001t0004g0038 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.25+3676T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274694 | ||||||
chr2:113274858
|
G | A | 17 | a0001c0001t0001g0127a0001c0001t0002g0131a0001c0001t0003g0008others(14): Show | 23 | HG00323.hp2 HG02071.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+3512C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274858 | ||||||
chr2:113274958
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.25+3412T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113274958 | ||||||
chr2:113275005
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.25+3365C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275005 | ||||||
chr2:113275190
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 187 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.25+3180A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275190 | ||||||
chr2:113275377
|
T | G | 1 | a0001c0001t0002g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+2993A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275377 | ||||||
chr2:113275546
|
A | G | 46 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0002g0004others(43): Show | 60 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.25+2824T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275546 | ||||||
chr2:113275573
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.25+2797C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275573 | ||||||
chr2:113275681
|
A | C | 1 | a0001c0001t0014g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25+2689T>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275681 | ||||||
chr2:113275752
|
G | A | 1 | a0001c0001t0003g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.25+2618C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275752 | ||||||
chr2:113275802
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.25+2568C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113275802 | ||||||
chr2:113276106
|
CTGGGGAA others(1): Show |
C | 3 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0022g0124 | 4 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+2256_25+2263del others(8): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276106 | ||||||
chr2:113276179
|
G | C | 1 | a0001c0001t0032g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25+2191C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276179 | ||||||
chr2:113276298
|
A | G | 1 | a0001c0001t0009g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.25+2072T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276298 | ||||||
chr2:113276582
|
T | C | 9 | a0001c0001t0002g0076a0001c0001t0002g0085a0001c0001t0004g0080others(6): Show | 9 | HG01109.hp1 HG02109.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+1788A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276582 | ||||||
chr2:113276585
|
T | G | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.25+1785A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276585 | ||||||
chr2:113276608
|
C | A | 121 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(118): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.25+1762G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276608 | ||||||
chr2:113276661
|
G | GA | 9 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+1708dupT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276661 | ||||||
chr2:113276661
|
GA | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(239): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.25+1708delT | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276661 | ||||||
chr2:113276838
|
AGCAGAAG others(20): Show |
A | 1 | a0001c0001t0002g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+1505_25+1531del others(27): Show |
PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276838 | ||||||
chr2:113276874
|
G | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0122others(4): Show | 10 | HG00639.hp2 HG02258.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+1496C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276874 | ||||||
chr2:113276964
|
G | A | 1 | a0001c0004t0007g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.25+1406C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113276964 | ||||||
chr2:113277050
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 125 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.25+1320C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277050 | ||||||
chr2:113277083
|
C | G | 122 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(119): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.25+1287G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277083 | ||||||
chr2:113277087
|
A | T | 1 | a0001c0001t0003g0140 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.25+1283T>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277087 | ||||||
chr2:113277095
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.25+1275C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277095 | ||||||
chr2:113277098
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.25+1272G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277098 | ||||||
chr2:113277153
|
T | C | 1 | a0001c0001t0016g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.25+1217A>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277153 | ||||||
chr2:113277156
|
G | A | 32 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0002g0034others(29): Show | 34 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(31): Show |
intron_variant | MODIFIER | c.25+1214C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277156 | ||||||
chr2:113277196
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0004g0035 | 2 | HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.25+1174T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277196 | ||||||
chr2:113277339
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0139others(48): Show | 63 | HG00544.hp2 HG00642.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.25+1031G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277339 | ||||||
chr2:113277375
|
C | T | 31 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.25+995G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277375 | ||||||
chr2:113277388
|
C | T | 4 | a0001c0001t0011g0024a0001c0001t0011g0025a0001c0001t0012g0022others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+982G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277388 | ||||||
chr2:113277404
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.25+966A>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277404 | ||||||
chr2:113277453
|
A | G | 1 | a0001c0001t0007g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.25+917T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277453 | ||||||
chr2:113277505
|
C | G | 1 | a0001c0001t0009g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.25+865G>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277505 | ||||||
chr2:113277580
|
A | G | 122 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(119): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.25+790T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277580 | ||||||
chr2:113277617
|
G | A | 148 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(145): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.25+753C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277617 | ||||||
chr2:113277752
|
G | A | 1 | a0001c0001t0019g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.25+618C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277752 | ||||||
chr2:113277779
|
G | T | 4 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0009g0031others(1): Show | 6 | HG02622.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+591C>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277779 | ||||||
chr2:113277785
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.25+585T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277785 | ||||||
chr2:113277874
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.25+496C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277874 | ||||||
chr2:113277888
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 125 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.25+482G>A | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277888 | ||||||
chr2:113277949
|
TG | T | 17 | a0001c0001t0001g0127a0001c0001t0002g0131a0001c0001t0003g0008others(14): Show | 23 | HG00323.hp2 HG02071.hp1 HG02698.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+420delC | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277949 | ||||||
chr2:113277952
|
G | C | 1 | a0001c0001t0001g0252 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.25+418C>G | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277952 | ||||||
chr2:113277991
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.25+379C>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113277991 | ||||||
chr2:113278173
|
C | A | 44 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0002g0004others(41): Show | 57 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.25+197G>T | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113278173 | ||||||
chr2:113278346
|
A | G | 105 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0061others(102): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.25+24T>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 2/11 | chr2 | 113278346 | ||||||
chr2:113278706
|
T | G | 1 | a0001c0001t0004g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-76+125A>C | PAX8 | ENSG00000125618.18 | transcript | ENST00000429538.8 | protein_coding | 1/11 | chr2 | 113278706 |