Item | Value |
---|---|
geneid | 5427 |
ensemblid | ENSG00000100479.14 |
hgncid | 9178 |
symbol | POLE2 |
name | DNA polymerase epsilon 2, accessory subunit |
refseq_nuc | NM_002692.4 |
refseq_prot | NP_002683.2 |
ensembl_nuc | ENST00000216367.10 |
ensembl_prot | ENSP00000216367.5 |
mane_status | MANE Select |
chr | chr14 |
start | 49643555 |
end | 49688214 |
strand | - |
ver | v1.2 |
region | chr14:49643555-49688214 |
region5000 | chr14:49638555-49693214 |
regionname0 | POLE2_chr14_49643555_49688214 |
regionname5000 | POLE2_chr14_49638555_49693214 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 527 | 228 | 93 | 50 | 49 | 14 | 20 | 30 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0002 | 0/0 | 527 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0003 | 0/0 | 527 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0004 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0005 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1584 | 168 | 48 | 40 | 49 | 12 | 17 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0002 | 0/0 | 1584 | 54 | 39 | 10 | 0 | 2 | 3 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0003 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0004 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0005 | 0/0 | 1584 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0006 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0007 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0008 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
c0009 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 109 | 180 | 62 | 38 | 49 | 12 | 17 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
t0002 | 0/0 | 109 | 48 | 31 | 11 | 3 | 1 | 2 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
t0003 | 0/0 | 109 | 4 | 1 | 1 | 0 | 1 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
t0004 | 0/0 | 107 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1584 | 168 | 48 | 40 | 49 | 12 | 17 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0002 | 0/0 | 1584 | 54 | 39 | 10 | 0 | 2 | 3 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0003 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0004 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0002c0006 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0002c0008 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0003c0005 | 0/0 | 1584 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0004c0009 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0005c0007 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1692 | 160 | 46 | 34 | 49 | 12 | 17 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0001t0002 | 0/0 | 1692 | 8 | 2 | 6 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0002t0001 | 0/0 | 1692 | 20 | 16 | 4 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0002t0002 | 0/0 | 1692 | 30 | 22 | 5 | 0 | 1 | 2 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0002t0003 | 0/0 | 1692 | 4 | 1 | 1 | 0 | 1 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0003t0002 | 0/0 | 1692 | 4 | 4 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0001c0004t0004 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0002c0006t0002 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0002c0008t0002 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0003c0005t0002 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0004c0009t0002 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
a0005c0007t0002 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | copy fasta | chr14 | 49638555 | 49693214 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0003t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0004t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0001c0004t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0002c0006t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0002c0008t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0003c0005t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0003c0005t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0004c0009t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
a0005c0007t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00597 | hp1 | a0003 | c0005 | t0002 | g0007 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0220 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0223 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01891 | hp1 | a0004 | c0009 | t0002 | g0228 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0162 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0222 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02615 | hp1 | a0002 | c0008 | t0002 | g0227 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0008 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0213 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03041 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03098 | hp1 | a0001 | c0004 | t0004 | g0086 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03098 | hp2 | a0001 | c0004 | t0004 | g0160 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03139 | hp2 | a0005 | c0007 | t0002 | g0161 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0224 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03453 | hp1 | a0001 | c0003 | t0002 | g0209 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18978 | hp2 | a0002 | c0006 | t0002 | g0005 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19011 | hp1 | a0003 | c0005 | t0002 | g0006 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0075 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0215 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0077 | REF | REF | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0172 | REF | REF | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:49650348
|
A | G | 1 | a0002 | 2 | HG02615.hp1 NA18978.hp2 |
missense_variant | MODERATE | c.1414T>C | p.Tyr472His | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/19 | 1425/1692 | 1414/1584 | 472/527 | chr14 | 49650348 | ||
chr14:49654789
|
G | C | 1 | a0003 | 2 | HG00597.hp1 NA19011.hp1 |
missense_variant | MODERATE | c.1068C>G | p.His356Gln | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/19 | 1079/1692 | 1068/1584 | 356/527 | chr14 | 49654789 | ||
chr14:49654814
|
A | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1043T>C | p.Ile348Thr | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/19 | 1054/1692 | 1043/1584 | 348/527 | chr14 | 49654814 | ||
chr14:49688169
|
G | A | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.35C>T | p.Ser12Phe | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/19 | 46/1692 | 35/1584 | 12/527 | chr14 | 49688169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:49665128
|
G | T | 8 | a0001c0002a0001c0003a0001c0004others(5): Show | 66 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(63): Show |
synonymous_variant | LOW | c.612C>A | p.Val204Val | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 8/19 | 623/1692 | 612/1584 | 204/527 | chr14 | 49665128 | ||
chr14:49666339
|
C | T | 2 | a0002c0006a0002c0008 | 2 | HG02615.hp1 NA18978.hp2 |
synonymous_variant | LOW | c.567G>A | p.Gln189Gln | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/19 | 578/1692 | 567/1584 | 189/527 | chr14 | 49666339 | ||
chr14:49666342
|
C | T | 2 | a0001c0003a0005c0007 | 5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.564G>A | p.Thr188Thr | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/19 | 575/1692 | 564/1584 | 188/527 | chr14 | 49666342 | ||
chr14:49669539
|
G | A | 1 | a0001c0004 | 2 | HG03098.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.477C>T | p.Ser159Ser | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/19 | 488/1692 | 477/1584 | 159/527 | chr14 | 49669539 | ||
chr14:49674162
|
T | C | 1 | a0003c0005 | 2 | HG00597.hp1 NA19011.hp1 |
synonymous_variant | LOW | c.378A>G | p.Lys126Lys | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/19 | 389/1692 | 378/1584 | 126/527 | chr14 | 49674162 | ||
chr14:49688174
|
C | G | 1 | a0002c0006 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.30G>C | p.Ala10Ala | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/19 | 41/1692 | 30/1584 | 10/527 | chr14 | 49688174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:49643601
|
T | C | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0003others(6): Show | 52 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*51A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 19/19 | 51 | chr14 | 49643601 | |||||
chr14:49643601
|
TAG | T | 1 | a0001c0004t0004 | 2 | HG03098.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49_*50delCT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 19/19 | 49 | chr14 | 49643601 | |||||
chr14:49643647
|
G | A | 1 | a0001c0002t0003 | 4 | HG00735.hp1 HG02145.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 19/19 | 5 | chr14 | 49643647 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:49643776
|
C | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-106G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643776 | ||||||
chr14:49643875
|
CT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1566-206delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643875 | ||||||
chr14:49643875
|
CTT | C | 18 | a0001c0002t0002g0013a0001c0002t0002g0030a0001c0002t0002g0031others(15): Show | 18 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1566-207_1566-206d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643875 | ||||||
chr14:49643896
|
T | C | 11 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(8): Show | 11 | HG01891.hp2 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1566-226A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643896 | ||||||
chr14:49643918
|
T | C | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-248A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643918 | ||||||
chr14:49643994
|
C | T | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1566-324G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643994 | ||||||
chr14:49644178
|
G | A | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-508C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644178 | ||||||
chr14:49644308
|
C | T | 5 | a0001c0001t0002g0065a0001c0002t0002g0205a0001c0002t0002g0216others(2): Show | 5 | HG00741.hp1 HG01167.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-638G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644308 | ||||||
chr14:49644309
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1566-639C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644309 | ||||||
chr14:49644403
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1566-733C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644403 | ||||||
chr14:49644474
|
C | T | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1566-804G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644474 | ||||||
chr14:49644491
|
CAA | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1566-823_1566-822d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644491 | ||||||
chr14:49644506
|
G | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1566-836C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644506 | ||||||
chr14:49644511
|
C | CA | 51 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(48): Show | 51 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1566-842dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644511 | ||||||
chr14:49644589
|
T | C | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1566-919A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644589 | ||||||
chr14:49644731
|
T | G | 12 | a0001c0001t0001g0027a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG01496.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1566-1061A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644731 | ||||||
chr14:49644956
|
C | T | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1566-1286G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644956 | ||||||
chr14:49645043
|
C | CA | 8 | a0001c0001t0001g0025a0001c0001t0001g0064a0001c0001t0001g0071others(5): Show | 8 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1566-1374dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAA | 11 | a0001c0002t0002g0013a0001c0002t0002g0030a0001c0002t0002g0031others(8): Show | 11 | HG00597.hp1 HG01891.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1566-1375_1566-137 others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAAA | 8 | a0001c0002t0002g0014a0001c0002t0002g0159a0001c0003t0002g0008others(5): Show | 8 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1566-1376_1566-137 others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAAAAAAA others(3): Show |
1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1566-1383_1566-137 others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAAAAAAA others(8): Show |
13 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0192others(10): Show | 13 | HG00735.hp1 HG01167.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1566-1388_1566-137 others(19): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAAAAAAA others(9): Show |
16 | a0001c0001t0002g0187a0001c0001t0002g0196a0001c0002t0002g0033others(13): Show | 16 | HG00741.hp1 HG01258.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1566-1374_1566-137 others(20): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0186a0001c0002t0003g0222 | 2 | HG02145.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1566-1374_1566-137 others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645043
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0002g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1566-1374_1566-137 others(22): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | ||||||
chr14:49645054
|
A | C | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1566-1384T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645054 | ||||||
chr14:49645059
|
C | A | 32 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(29): Show | 32 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1566-1389G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645059 | ||||||
chr14:49645115
|
G | C | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-1445C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645115 | ||||||
chr14:49645262
|
TCAC | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-1595_1566-159 others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645262 | ||||||
chr14:49645349
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(137): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1566-1679G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645349 | ||||||
chr14:49645475
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1566-1805G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645475 | ||||||
chr14:49645499
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1565+1794C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645499 | ||||||
chr14:49645657
|
C | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1636G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645657 | ||||||
chr14:49645761
|
C | A | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1532G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645761 | ||||||
chr14:49645883
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1565+1410A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645883 | ||||||
chr14:49645915
|
G | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0002t0001g0002others(16): Show | 20 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1565+1378C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645915 | ||||||
chr14:49645994
|
G | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(56): Show | 62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1565+1299C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645994 | ||||||
chr14:49646171
|
A | G | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1122T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646171 | ||||||
chr14:49646226
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1565+1067C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646226 | ||||||
chr14:49646290
|
G | GC | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1002_1565+100 others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646290 | ||||||
chr14:49646302
|
G | GT | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(42): Show | 47 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1565+990dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
G | GTT | 20 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0028others(17): Show | 20 | HG00438.hp2 HG01261.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.1565+989_1565+990d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
G | GTTT | 12 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0047others(9): Show | 12 | HG00099.hp2 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1565+988_1565+990d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
G | GTTTT | 5 | a0001c0001t0001g0050a0001c0001t0001g0073a0001c0001t0001g0091others(2): Show | 5 | HG00280.hp1 HG01192.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1565+987_1565+990d others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
G | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0084 | 3 | HG02630.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1565+991C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GT | G | 8 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0088others(5): Show | 8 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1565+990delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GTTT | G | 14 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0002t0001g0002others(11): Show | 15 | HG00733.hp2 HG01361.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1565+988_1565+990d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GTTTTTTT others(1): Show |
G | 5 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0035others(2): Show | 5 | HG00597.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+983_1565+990d others(10): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GTTTTTTT others(2): Show |
G | 8 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0157others(5): Show | 8 | HG01891.hp2 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1565+982_1565+990d others(11): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1565+976_1565+990d others(17): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GTTTTTTT others(9): Show |
G | 18 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0048others(15): Show | 21 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1565+975_1565+990d others(18): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646302
|
GTTTTTTT others(12): Show |
G | 3 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0078 | 3 | HG00741.hp2 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1565+972_1565+990d others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | ||||||
chr14:49646310
|
T | TG | 9 | a0001c0001t0002g0188a0001c0001t0002g0196a0001c0002t0002g0033others(6): Show | 9 | HG00741.hp1 HG01258.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565+982_1565+983i others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646310 | ||||||
chr14:49646311
|
T | G | 24 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(21): Show | 24 | HG00735.hp1 HG01167.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1565+982A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646311 | ||||||
chr14:49646312
|
T | G | 5 | a0001c0003t0002g0009a0001c0003t0002g0209a0002c0006t0002g0005others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+981A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646312 | ||||||
chr14:49646346
|
C | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+947G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646346 | ||||||
chr14:49646472
|
G | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1565+821C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646472 | ||||||
chr14:49646553
|
G | C | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+740C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646553 | ||||||
chr14:49646573
|
G | A | 2 | a0001c0001t0001g0044a0001c0002t0002g0031 | 2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1565+720C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646573 | ||||||
chr14:49646643
|
G | A | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0035others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565+650C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646643 | ||||||
chr14:49646664
|
C | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+629G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646664 | ||||||
chr14:49646678
|
A | G | 11 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(8): Show | 11 | HG01891.hp2 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1565+615T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646678 | ||||||
chr14:49647114
|
A | G | 75 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0002g0065others(72): Show | 76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1565+179T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647114 | ||||||
chr14:49647170
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1565+123T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647170 | ||||||
chr14:49647191
|
T | C | 1 | a0001c0002t0002g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1565+102A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647191 | ||||||
chr14:49647197
|
T | G | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+96A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647197 | ||||||
chr14:49647230
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1565+63A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647230 | ||||||
chr14:49647399
|
CT | C | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1498-40delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647399 | ||||||
chr14:49647407
|
T | A | 7 | a0001c0002t0002g0162a0001c0003t0002g0008a0001c0003t0002g0009others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-47A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647407 | ||||||
chr14:49647461
|
A | AT | 3 | a0001c0002t0002g0014a0001c0004t0004g0086a0003c0005t0002g0007 | 3 | HG00597.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1498-102dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647461 | ||||||
chr14:49647465
|
A | T | 16 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(13): Show | 16 | HG00597.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1498-105T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647465 | ||||||
chr14:49647465
|
AT | A | 5 | a0001c0002t0002g0162a0001c0003t0002g0008a0001c0003t0002g0009others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-106delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647465 | ||||||
chr14:49647541
|
T | C | 32 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(29): Show | 32 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1498-181A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647541 | ||||||
chr14:49647557
|
G | C | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0035others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498-197C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647557 | ||||||
chr14:49647642
|
G | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1498-282C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647642 | ||||||
chr14:49647860
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1498-500G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647860 | ||||||
chr14:49648008
|
C | T | 1 | a0001c0002t0002g0135 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1498-648G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648008 | ||||||
chr14:49648083
|
T | G | 52 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(49): Show | 52 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1498-723A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648083 | ||||||
chr14:49648122
|
C | A | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1498-762G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648122 | ||||||
chr14:49648174
|
A | G | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1498-814T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648174 | ||||||
chr14:49648228
|
C | T | 13 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(10): Show | 13 | HG00597.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1498-868G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648228 | ||||||
chr14:49648320
|
G | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1498-960C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648320 | ||||||
chr14:49648636
|
C | T | 5 | a0001c0002t0002g0162a0001c0003t0002g0008a0001c0003t0002g0009others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-1276G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648636 | ||||||
chr14:49648731
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1498-1371G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648731 | ||||||
chr14:49648881
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1497+1384C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648881 | ||||||
chr14:49648984
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1497+1281T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648984 | ||||||
chr14:49649022
|
A | G | 3 | a0001c0002t0002g0217a0001c0002t0002g0218a0001c0002t0002g0219 | 3 | HG02559.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1497+1243T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649022 | ||||||
chr14:49649137
|
C | CT | 28 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0071others(25): Show | 28 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1497+1127dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | ||||||
chr14:49649137
|
C | CTT | 7 | a0001c0001t0001g0141a0001c0002t0001g0010a0001c0002t0001g0012others(4): Show | 7 | HG01358.hp1 HG01361.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+1126_1497+112 others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | ||||||
chr14:49649137
|
CTTT | C | 9 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(6): Show | 9 | HG02258.hp2 HG02630.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+1125_1497+112 others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | ||||||
chr14:49649137
|
CTTTT | C | 30 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1497+1124_1497+112 others(8): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | ||||||
chr14:49649137
|
CTTTTT | C | 8 | a0001c0002t0002g0162a0001c0002t0002g0216a0001c0003t0002g0008others(5): Show | 8 | HG01167.hp2 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+1123_1497+112 others(9): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | ||||||
chr14:49649302
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1497+963A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649302 | ||||||
chr14:49649349
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0155 | 2 | HG00642.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1497+916A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649349 | ||||||
chr14:49649436
|
A | G | 3 | a0001c0001t0001g0169a0001c0002t0001g0017a0001c0002t0001g0018 | 3 | HG01361.hp2 HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1497+829T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649436 | ||||||
chr14:49649438
|
A | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1497+827T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649438 | ||||||
chr14:49649453
|
C | T | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1497+812G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649453 | ||||||
chr14:49649597
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1497+668C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649597 | ||||||
chr14:49649640
|
G | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1497+625C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649640 | ||||||
chr14:49649740
|
T | C | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1497+525A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649740 | ||||||
chr14:49649745
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+520C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649745 | ||||||
chr14:49649985
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1497+280G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649985 | ||||||
chr14:49650034
|
G | T | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1497+231C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49650034 | ||||||
chr14:49650144
|
G | A | 41 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(38): Show | 41 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1497+121C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49650144 | ||||||
chr14:49650248
|
A | G | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1497+17T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49650248 | ||||||
chr14:49651070
|
C | T | 75 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0002g0065others(72): Show | 76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1320+199G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651070 | ||||||
chr14:49651071
|
TAA | T | 75 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0002g0065others(72): Show | 76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1320+196_1320+197d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651071 | ||||||
chr14:49651077
|
A | C | 75 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0002g0065others(72): Show | 76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1320+192T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651077 | ||||||
chr14:49651087
|
A | C | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1320+182T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651087 | ||||||
chr14:49651119
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1320+150T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651119 | ||||||
chr14:49651138
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0180 | 2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1320+131G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651138 | ||||||
chr14:49651160
|
T | C | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1320+109A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651160 | ||||||
chr14:49651233
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0112 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1320+36A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651233 | ||||||
chr14:49651515
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1212-138G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651515 | ||||||
chr14:49651641
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1212-264T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651641 | ||||||
chr14:49651692
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1212-315T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651692 | ||||||
chr14:49651942
|
G | A | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1212-565C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651942 | ||||||
chr14:49652058
|
GGGGTCCC others(12): Show |
G | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1212-700_1212-682d others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652058 | ||||||
chr14:49652112
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0141others(2): Show | 6 | HG02559.hp2 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-735C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652112 | ||||||
chr14:49652123
|
T | C | 21 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0002t0001g0002others(18): Show | 22 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1212-746A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652123 | ||||||
chr14:49652152
|
TAAGAATA others(150): Show |
T | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0020others(152): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1212-932_1212-776d others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652152 | ||||||
chr14:49652165
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1212-788G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652165 | ||||||
chr14:49652219
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0076 | 2 | HG02080.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1212-842C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652219 | ||||||
chr14:49652263
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0107 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1212-896_1212-887d others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0180 | 2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1212-898_1212-887d others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0184 | 2 | HG03927.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1212-899_1212-887d others(15): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0142others(2): Show | 6 | HG00438.hp1 HG00438.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-897_1212-887d others(13): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0045a0001c0001t0001g0078a0001c0001t0001g0098others(2): Show | 5 | HG00741.hp2 HG01346.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-898_1212-887d others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1212-899_1212-887d others(15): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1212-900_1212-887d others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1212-901_1212-887d others(17): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0022a0001c0001t0001g0052 | 2 | NA18979.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1212-902_1212-887d others(18): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(10): Show |
C | 6 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0108others(3): Show | 6 | HG00597.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-903_1212-887d others(19): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(11): Show |
C | 15 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0027others(12): Show | 15 | HG00544.hp2 HG00673.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212-904_1212-887d others(20): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0190 | 3 | HG02040.hp1 HG02040.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1212-905_1212-887d others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(17): Show |
C | 1 | a0001c0001t0001g0025 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1212-910_1212-887d others(26): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1212-911_1212-887d others(27): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1212-913_1212-887d others(29): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(22): Show |
C | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1212-915_1212-887d others(31): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652263
|
CAAAAAAA others(26): Show |
C | 2 | a0001c0001t0001g0089a0001c0001t0001g0191 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.1212-919_1212-887d others(35): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | ||||||
chr14:49652311
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0166 | 2 | HG00621.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1212-934T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652311 | ||||||
chr14:49652426
|
G | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1212-1049C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652426 | ||||||
chr14:49652646
|
T | A | 5 | a0001c0002t0002g0162a0001c0003t0002g0008a0001c0003t0002g0009others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-1269A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652646 | ||||||
chr14:49652747
|
T | C | 32 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(29): Show | 32 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1211+1243A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652747 | ||||||
chr14:49652856
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1211+1134G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652856 | ||||||
chr14:49652918
|
G | C | 1 | a0001c0002t0002g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1211+1072C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652918 | ||||||
chr14:49652974
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1211+1016A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652974 | ||||||
chr14:49652975
|
T | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1211+1015A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652975 | ||||||
chr14:49653194
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1211+796C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653194 | ||||||
chr14:49653431
|
G | A | 54 | a0001c0001t0002g0065a0001c0001t0002g0185a0001c0001t0002g0186others(51): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211+559C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653431 | ||||||
chr14:49653565
|
T | C | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1211+425A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653565 | ||||||
chr14:49653576
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1211+414T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653576 | ||||||
chr14:49653779
|
A | AG | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1211+210_1211+211i others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653779 | ||||||
chr14:49654140
|
C | T | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1133+15G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 14/18 | chr14 | 49654140 | ||||||
chr14:49654318
|
C | T | 2 | a0001c0002t0002g0135a0001c0002t0002g0181 | 2 | HG01258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1074-104G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/18 | chr14 | 49654318 | ||||||
chr14:49654419
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1074-205A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/18 | chr14 | 49654419 | ||||||
chr14:49654731
|
G | GT | 11 | a0001c0001t0001g0037a0001c0002t0002g0162a0001c0003t0002g0008others(8): Show | 11 | HG00597.hp1 HG02055.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1073+52dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/18 | chr14 | 49654731 | ||||||
chr14:49655458
|
A | AAC | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(15): Show | 20 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.928+211_928+212dup others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACAC | 3 | a0001c0001t0001g0123a0001c0002t0002g0162a0001c0003t0002g0209 | 3 | HG02055.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.928+209_928+212dup others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACACAC | 11 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0002g0030others(8): Show | 11 | HG01361.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.928+207_928+212dup others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACACACA others(1): Show |
3 | a0001c0002t0001g0015a0001c0002t0002g0013a0001c0002t0002g0014 | 3 | HG02258.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.928+205_928+212dup others(8): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACACACA others(3): Show |
2 | a0001c0002t0001g0088a0001c0002t0001g0152 | 2 | HG01099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.928+203_928+212dup others(10): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACACACA others(5): Show |
10 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0016others(7): Show | 10 | HG00733.hp2 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.928+201_928+212dup others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACACACA others(7): Show |
4 | a0001c0002t0001g0002a0001c0002t0001g0012a0001c0002t0001g0039others(1): Show | 5 | HG01358.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+199_928+212dup others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.928+197_928+212dup others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
A | AC | 2 | a0001c0001t0001g0090a0001c0001t0001g0121 | 2 | HG01261.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.928+212_928+213ins others(1): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
AAC | A | 34 | a0001c0001t0001g0122a0001c0001t0002g0185a0001c0001t0002g0186others(31): Show | 34 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.928+211_928+212del others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655458
|
AACAC | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0134others(1): Show | 4 | HG00140.hp1 HG01099.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+209_928+212del others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | ||||||
chr14:49655468
|
C | T | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.928+203G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655468 | ||||||
chr14:49655540
|
T | C | 38 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(35): Show | 38 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.928+131A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655540 | ||||||
chr14:49655562
|
C | CAG | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.928+108_928+109ins others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655562 | ||||||
chr14:49655628
|
C | A | 1 | a0001c0002t0002g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.928+43G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655628 | ||||||
chr14:49655634
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.928+37T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655634 | ||||||
chr14:49656041
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0165 | 2 | NA19000.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.756-198A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656041 | ||||||
chr14:49656051
|
C | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.756-208G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656051 | ||||||
chr14:49656078
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0132 | 3 | HG01361.hp1 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.756-235C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656078 | ||||||
chr14:49656223
|
C | T | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.756-380G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656223 | ||||||
chr14:49656281
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.756-438C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656281 | ||||||
chr14:49656327
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.756-484T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656327 | ||||||
chr14:49656354
|
C | CA | 19 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0044others(16): Show | 19 | HG00558.hp2 HG01081.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.756-512dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656354 | ||||||
chr14:49656354
|
CA | C | 55 | a0001c0001t0001g0091a0001c0001t0001g0139a0001c0001t0002g0185others(52): Show | 55 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.756-512delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656354 | ||||||
chr14:49656366
|
A | C | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-523T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656366 | ||||||
chr14:49656370
|
A | G | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.756-527T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656370 | ||||||
chr14:49656430
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756-587C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656430 | ||||||
chr14:49656575
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.756-732A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656575 | ||||||
chr14:49656759
|
T | G | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.756-916A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656759 | ||||||
chr14:49657048
|
G | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.756-1205C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657048 | ||||||
chr14:49657107
|
T | C | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-1264A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657107 | ||||||
chr14:49657112
|
C | CA | 32 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0022others(29): Show | 34 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.756-1270dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657112 | ||||||
chr14:49657112
|
C | CAA | 41 | a0001c0001t0001g0120a0001c0001t0002g0185a0001c0001t0002g0186others(38): Show | 41 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.756-1271_756-1270d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657112 | ||||||
chr14:49657112
|
CA | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0141others(8): Show | 12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.756-1270delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657112 | ||||||
chr14:49657199
|
G | A | 3 | a0001c0002t0002g0217a0001c0002t0002g0218a0001c0002t0002g0219 | 3 | HG02559.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.756-1356C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657199 | ||||||
chr14:49657301
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756-1458A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657301 | ||||||
chr14:49657405
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.756-1562A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657405 | ||||||
chr14:49657429
|
CT | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0116others(13): Show | 16 | HG00597.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.756-1587delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657429 | ||||||
chr14:49657455
|
C | T | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-1612G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657455 | ||||||
chr14:49657503
|
C | T | 1 | a0001c0002t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.756-1660G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657503 | ||||||
chr14:49657814
|
T | C | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-1971A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657814 | ||||||
chr14:49658003
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.756-2160G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658003 | ||||||
chr14:49658076
|
C | CT | 20 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(17): Show | 21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.756-2234dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658076 | ||||||
chr14:49658375
|
C | G | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-2532G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658375 | ||||||
chr14:49658424
|
G | A | 20 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(17): Show | 21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.756-2581C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658424 | ||||||
chr14:49658506
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.756-2663G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658506 | ||||||
chr14:49658595
|
G | A | 72 | a0001c0001t0001g0037a0001c0001t0002g0185a0001c0001t0002g0186others(69): Show | 73 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.756-2752C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658595 | ||||||
chr14:49658611
|
G | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.756-2768C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658611 | ||||||
chr14:49659161
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.756-3318T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659161 | ||||||
chr14:49659263
|
A | AT | 73 | a0001c0001t0001g0037a0001c0001t0002g0185a0001c0001t0002g0186others(70): Show | 74 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-3421dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659263 | ||||||
chr14:49659302
|
G | T | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.756-3459C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659302 | ||||||
chr14:49659346
|
G | A | 51 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(48): Show | 51 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.756-3503C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659346 | ||||||
chr14:49659435
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.756-3592G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659435 | ||||||
chr14:49659494
|
A | G | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-3651T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659494 | ||||||
chr14:49659654
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.755+3661G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659654 | ||||||
chr14:49659723
|
G | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+3592C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659723 | ||||||
chr14:49660176
|
G | T | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+3139C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660176 | ||||||
chr14:49660299
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01496.hp2 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.755+3016G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660299 | ||||||
chr14:49660326
|
T | A | 6 | a0001c0002t0002g0162a0001c0003t0002g0008a0001c0003t0002g0009others(3): Show | 6 | HG02055.hp1 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+2989A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660326 | ||||||
chr14:49660558
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.755+2757C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660558 | ||||||
chr14:49660657
|
C | T | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+2658G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660657 | ||||||
chr14:49660712
|
C | T | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+2603G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660712 | ||||||
chr14:49660813
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.755+2502T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660813 | ||||||
chr14:49660852
|
T | C | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.755+2463A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660852 | ||||||
chr14:49660873
|
A | G | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+2442T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660873 | ||||||
chr14:49660886
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.755+2429G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660886 | ||||||
chr14:49660925
|
A | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.755+2390T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660925 | ||||||
chr14:49661141
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.755+2174C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661141 | ||||||
chr14:49661177
|
T | C | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+2138A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661177 | ||||||
chr14:49661214
|
CA | C | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+2100delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661214 | ||||||
chr14:49661387
|
G | A | 53 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(50): Show | 53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+1928C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661387 | ||||||
chr14:49661548
|
G | A | 30 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.755+1767C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661548 | ||||||
chr14:49661825
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.755+1490G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661825 | ||||||
chr14:49661953
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.755+1362A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661953 | ||||||
chr14:49661964
|
C | A | 1 | a0001c0003t0002g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.755+1351G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661964 | ||||||
chr14:49661970
|
G | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0191 | 3 | HG00438.hp2 HG00558.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.755+1345C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661970 | ||||||
chr14:49662134
|
T | G | 5 | a0001c0002t0002g0174a0001c0002t0002g0175a0001c0002t0002g0176others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+1181A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662134 | ||||||
chr14:49662140
|
T | C | 5 | a0001c0002t0002g0174a0001c0002t0002g0175a0001c0002t0002g0176others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+1175A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662140 | ||||||
chr14:49662233
|
A | C | 1 | a0004c0009t0002g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.755+1082T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662233 | ||||||
chr14:49662301
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.755+1014G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662301 | ||||||
chr14:49662311
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.755+1004C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662311 | ||||||
chr14:49662333
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.755+982G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662333 | ||||||
chr14:49662649
|
G | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.755+666C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662649 | ||||||
chr14:49662797
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(138): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.755+518T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662797 | ||||||
chr14:49662803
|
A | G | 1 | a0001c0002t0002g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.755+512T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662803 | ||||||
chr14:49662830
|
T | C | 73 | a0001c0001t0001g0037a0001c0001t0002g0185a0001c0001t0002g0186others(70): Show | 74 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.755+485A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662830 | ||||||
chr14:49663128
|
T | A | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.755+187A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49663128 | ||||||
chr14:49663223
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0195others(1): Show | 4 | HG01168.hp1 HG01192.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+92G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49663223 | ||||||
chr14:49663468
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.683-81A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663468 | ||||||
chr14:49663614
|
T | C | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.683-227A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663614 | ||||||
chr14:49663766
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.683-379A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663766 | ||||||
chr14:49663803
|
C | T | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0035others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-416G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663803 | ||||||
chr14:49663961
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | NA18979.hp2 NA18988.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-574G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663961 | ||||||
chr14:49663962
|
G | A | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-575C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663962 | ||||||
chr14:49664041
|
GA | G | 52 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(49): Show | 52 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.682+584delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664041 | ||||||
chr14:49664192
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.682+434T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664192 | ||||||
chr14:49664193
|
C | T | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.682+433G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664193 | ||||||
chr14:49664214
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.682+412A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664214 | ||||||
chr14:49664218
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.682+408T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664218 | ||||||
chr14:49664219
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.682+407A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664219 | ||||||
chr14:49664360
|
G | GA | 24 | a0001c0001t0001g0037a0001c0001t0001g0120a0001c0001t0001g0165others(21): Show | 25 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.682+265dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664360 | ||||||
chr14:49664777
|
C | G | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.634-103G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 8/18 | chr14 | 49664777 | ||||||
chr14:49665010
|
T | C | 45 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(42): Show | 45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.633+97A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 8/18 | chr14 | 49665010 | ||||||
chr14:49665214
|
T | C | 23 | a0001c0002t0002g0033a0001c0002t0002g0075a0001c0002t0002g0135others(20): Show | 23 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.577-51A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665214 | ||||||
chr14:49665550
|
A | G | 40 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(37): Show | 40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.577-387T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665550 | ||||||
chr14:49665644
|
T | G | 5 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(2): Show | 6 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-481A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665644 | ||||||
chr14:49665677
|
G | GT | 10 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0072others(7): Show | 10 | HG01891.hp1 HG01978.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-515dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665677 | ||||||
chr14:49665821
|
A | T | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.576+509T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665821 | ||||||
chr14:49665822
|
T | TA | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.576+507_576+508ins others(1): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665822 | ||||||
chr14:49665831
|
T | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0131a0001c0001t0001g0148others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+499A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665831 | ||||||
chr14:49666185
|
AT | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.576+144delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49666185 | ||||||
chr14:49666231
|
T | G | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.576+99A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49666231 | ||||||
chr14:49666315
|
T | C | 43 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(40): Show | 43 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.576+15A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49666315 | ||||||
chr14:49666500
|
T | C | 45 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(42): Show | 45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.493-87A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666500 | ||||||
chr14:49666573
|
T | C | 43 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(40): Show | 43 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.493-160A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666573 | ||||||
chr14:49666651
|
G | C | 1 | a0002c0008t0002g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.493-238C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666651 | ||||||
chr14:49666729
|
GAA | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-318_493-317del others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666729 | ||||||
chr14:49666914
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0063others(1): Show | 4 | HG01433.hp1 HG01884.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-501A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666914 | ||||||
chr14:49667086
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.493-673C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667086 | ||||||
chr14:49667142
|
C | T | 11 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(8): Show | 12 | HG00733.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.493-729G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667142 | ||||||
chr14:49667184
|
C | CA | 8 | a0001c0001t0001g0057a0001c0001t0001g0076a0001c0001t0001g0108others(5): Show | 8 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-772dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667184 | ||||||
chr14:49667198
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.493-785T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667198 | ||||||
chr14:49667487
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.493-1074A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667487 | ||||||
chr14:49667552
|
C | CT | 41 | a0001c0001t0001g0180a0001c0002t0002g0013a0001c0002t0002g0014others(38): Show | 41 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.493-1140dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667552 | ||||||
chr14:49667552
|
C | CTT | 5 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0209others(2): Show | 5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-1141_493-1140d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667552 | ||||||
chr14:49667843
|
T | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.493-1430A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667843 | ||||||
chr14:49667917
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0002g0065 | 2 | HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.493-1504A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667917 | ||||||
chr14:49667994
|
G | A | 1 | a0001c0002t0002g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.492+1530C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667994 | ||||||
chr14:49668154
|
T | G | 1 | a0001c0004t0004g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.492+1370A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668154 | ||||||
chr14:49668251
|
CAG | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.492+1271_492+1272d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668251 | ||||||
chr14:49668289
|
G | A | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.492+1235C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668289 | ||||||
chr14:49668558
|
A | T | 31 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(28): Show | 31 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.492+966T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668558 | ||||||
chr14:49668855
|
C | T | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.492+669G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668855 | ||||||
chr14:49668856
|
A | G | 43 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(40): Show | 43 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.492+668T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668856 | ||||||
chr14:49668958
|
G | A | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.492+566C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668958 | ||||||
chr14:49668999
|
A | G | 45 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(42): Show | 45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.492+525T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668999 | ||||||
chr14:49669175
|
T | C | 5 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0209others(2): Show | 5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+349A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669175 | ||||||
chr14:49669277
|
G | T | 5 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0209others(2): Show | 5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+247C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669277 | ||||||
chr14:49669302
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.492+222G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669302 | ||||||
chr14:49669407
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+117A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669407 | ||||||
chr14:49669640
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0194 | 3 | HG00609.hp1 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.418-42A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669640 | ||||||
chr14:49669667
|
G | A | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.418-69C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669667 | ||||||
chr14:49669711
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.418-113A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669711 | ||||||
chr14:49669781
|
G | A | 45 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(42): Show | 45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.418-183C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669781 | ||||||
chr14:49669842
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.418-244G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669842 | ||||||
chr14:49669858
|
C | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0210 | 2 | HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.418-260G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669858 | ||||||
chr14:49669882
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.418-284A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669882 | ||||||
chr14:49669891
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.418-293C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669891 | ||||||
chr14:49670081
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.418-483G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670081 | ||||||
chr14:49670304
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0124 | 2 | HG02976.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.418-706C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670304 | ||||||
chr14:49670317
|
C | CA | 26 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0026others(23): Show | 27 | HG00609.hp1 HG00733.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.418-720dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
C | CAA | 23 | a0001c0001t0001g0077a0001c0002t0001g0017a0001c0002t0001g0018others(20): Show | 23 | HG01361.hp2 HG01515.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.418-721_418-720dup others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
C | CAAA | 8 | a0001c0002t0002g0033a0001c0002t0002g0035a0001c0002t0002g0135others(5): Show | 8 | HG00741.hp1 HG01258.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.418-722_418-720dup others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
C | CAAAAA | 6 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0012others(3): Show | 6 | HG00735.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-724_418-720dup others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
C | CAAAAAAA | 5 | a0001c0001t0001g0037a0001c0002t0001g0016a0001c0002t0001g0038others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.418-726_418-720dup others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
CA | C | 10 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0079others(7): Show | 10 | HG00099.hp1 HG00099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.418-720delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
CAAAAAAA | C | 9 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0110others(6): Show | 9 | HG00639.hp1 HG00642.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-726_418-720del others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
CAAAAAAA others(1): Show |
C | 55 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.418-727_418-720del others(8): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0002g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.418-729_418-720del others(10): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0004t0004g0086a0002c0006t0002g0005a0002c0008t0002g0227others(1): Show | 4 | HG00597.hp1 HG02615.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-730_418-720del others(11): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670317
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0004g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.418-731_418-720del others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | ||||||
chr14:49670447
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.418-849C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670447 | ||||||
chr14:49670579
|
A | G | 1 | a0003c0005t0002g0006 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.418-981T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670579 | ||||||
chr14:49670662
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.418-1064C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670662 | ||||||
chr14:49670706
|
A | G | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.418-1108T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670706 | ||||||
chr14:49670774
|
G | C | 43 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(40): Show | 43 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.418-1176C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670774 | ||||||
chr14:49670982
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.418-1384A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670982 | ||||||
chr14:49671230
|
T | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.418-1632A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671230 | ||||||
chr14:49671296
|
C | A | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.418-1698G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671296 | ||||||
chr14:49671339
|
T | C | 43 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(40): Show | 43 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.418-1741A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671339 | ||||||
chr14:49671390
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.418-1792C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671390 | ||||||
chr14:49671514
|
G | T | 1 | a0001c0002t0002g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.418-1916C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671514 | ||||||
chr14:49671536
|
G | C | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.418-1938C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671536 | ||||||
chr14:49671618
|
G | GA | 19 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0050others(16): Show | 19 | HG00597.hp1 HG00621.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.418-2021dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671618 | ||||||
chr14:49671618
|
G | GAA | 30 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.418-2022_418-2021d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671618 | ||||||
chr14:49671618
|
G | GAAA | 10 | a0001c0002t0001g0039a0001c0002t0002g0013a0001c0002t0002g0014others(7): Show | 10 | HG01358.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.418-2023_418-2021d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671618 | ||||||
chr14:49671692
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0202 | 2 | HG00438.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.418-2094A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671692 | ||||||
chr14:49671784
|
G | A | 10 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0157others(7): Show | 10 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.418-2186C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671784 | ||||||
chr14:49672040
|
T | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0150others(1): Show | 4 | HG00621.hp2 HG00673.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.417+2083A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672040 | ||||||
chr14:49672077
|
G | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG01496.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.417+2046C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672077 | ||||||
chr14:49672253
|
T | G | 1 | a0001c0001t0002g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.417+1870A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672253 | ||||||
chr14:49672284
|
A | G | 45 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(42): Show | 45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.417+1839T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672284 | ||||||
chr14:49672396
|
CTTTA | C | 39 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(36): Show | 39 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.417+1723_417+1726d others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672396 | ||||||
chr14:49672402
|
T | C | 21 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(18): Show | 22 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.417+1721A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672402 | ||||||
chr14:49672501
|
CT | C | 42 | a0001c0001t0001g0028a0001c0002t0002g0030a0001c0002t0002g0031others(39): Show | 42 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.417+1621delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672501 | ||||||
chr14:49672585
|
C | T | 5 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(2): Show | 5 | HG01258.hp2 HG01978.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+1538G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672585 | ||||||
chr14:49672801
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.417+1322G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672801 | ||||||
chr14:49672923
|
T | C | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.417+1200A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672923 | ||||||
chr14:49672996
|
C | T | 1 | a0002c0006t0002g0005 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.417+1127G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672996 | ||||||
chr14:49673122
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.417+1001A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673122 | ||||||
chr14:49673564
|
T | C | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.417+559A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673564 | ||||||
chr14:49673569
|
A | G | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.417+554T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673569 | ||||||
chr14:49673671
|
G | A | 39 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(36): Show | 39 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.417+452C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673671 | ||||||
chr14:49673671
|
G | C | 3 | a0001c0003t0002g0209a0001c0003t0002g0213a0005c0007t0002g0161 | 3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.417+452C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673671 | ||||||
chr14:49673695
|
G | A | 40 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0030others(37): Show | 40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.417+428C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673695 | ||||||
chr14:49673740
|
G | A | 3 | a0001c0002t0002g0162a0002c0006t0002g0005a0002c0008t0002g0227 | 3 | HG02055.hp1 HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.417+383C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673740 | ||||||
chr14:49674510
|
A | C | 4 | a0001c0004t0004g0086a0001c0004t0004g0160a0003c0005t0002g0006others(1): Show | 4 | HG00597.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-83T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674510 | ||||||
chr14:49674540
|
C | G | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-113G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674540 | ||||||
chr14:49674606
|
C | G | 64 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(61): Show | 65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-179G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674606 | ||||||
chr14:49674607
|
T | C | 64 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(61): Show | 65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-180A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674607 | ||||||
chr14:49674730
|
T | C | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-303A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674730 | ||||||
chr14:49674900
|
G | A | 20 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(17): Show | 21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.246-473C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674900 | ||||||
chr14:49675088
|
A | AT | 60 | a0001c0001t0001g0037a0001c0001t0001g0101a0001c0002t0001g0002others(57): Show | 61 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-662dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675088 | ||||||
chr14:49675098
|
T | TC | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-672_246-671ins others(1): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675098 | ||||||
chr14:49675171
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG00280.hp2 HG01074.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-744C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675171 | ||||||
chr14:49675242
|
G | A | 3 | a0001c0003t0002g0209a0001c0003t0002g0213a0005c0007t0002g0161 | 3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-815C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675242 | ||||||
chr14:49675363
|
C | A | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.246-936G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675363 | ||||||
chr14:49675462
|
GAC | G | 2 | a0001c0004t0004g0086a0001c0004t0004g0160 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-1037_246-1036d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675462 | ||||||
chr14:49675519
|
C | T | 60 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(57): Show | 61 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-1092G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675519 | ||||||
chr14:49675636
|
G | A | 60 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(57): Show | 61 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-1209C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675636 | ||||||
chr14:49675668
|
C | T | 3 | a0001c0003t0002g0209a0001c0003t0002g0213a0005c0007t0002g0161 | 3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-1241G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675668 | ||||||
chr14:49675669
|
G | A | 2 | a0001c0002t0003g0220a0001c0002t0003g0224 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.246-1242C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675669 | ||||||
chr14:49676074
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.246-1647C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676074 | ||||||
chr14:49676085
|
A | G | 2 | a0001c0003t0002g0209a0001c0003t0002g0213 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-1658T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676085 | ||||||
chr14:49676163
|
T | C | 2 | a0001c0002t0001g0011a0001c0002t0001g0012 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.246-1736A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676163 | ||||||
chr14:49676255
|
C | T | 64 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(61): Show | 65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-1828G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676255 | ||||||
chr14:49676495
|
C | T | 64 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(61): Show | 65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-2068G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676495 | ||||||
chr14:49676500
|
G | T | 1 | a0004c0009t0002g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.246-2073C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676500 | ||||||
chr14:49676540
|
T | C | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.246-2113A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676540 | ||||||
chr14:49676685
|
G | C | 1 | a0001c0002t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.246-2258C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676685 | ||||||
chr14:49676761
|
A | G | 64 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(61): Show | 65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-2334T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676761 | ||||||
chr14:49676785
|
T | G | 64 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(61): Show | 65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-2358A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676785 | ||||||
chr14:49676945
|
A | G | 1 | a0001c0002t0002g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.246-2518T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676945 | ||||||
chr14:49676971
|
G | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.246-2544C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676971 | ||||||
chr14:49677014
|
G | T | 2 | a0001c0003t0002g0209a0001c0003t0002g0213 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-2587C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677014 | ||||||
chr14:49677082
|
G | C | 3 | a0001c0001t0001g0164a0003c0005t0002g0006a0003c0005t0002g0007 | 3 | HG00597.hp1 HG02040.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.245+2643C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677082 | ||||||
chr14:49677100
|
C | T | 1 | a0001c0002t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.245+2625G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677100 | ||||||
chr14:49677241
|
G | T | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245+2484C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677241 | ||||||
chr14:49677248
|
G | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0014 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245+2477C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677248 | ||||||
chr14:49677325
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.245+2400C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677325 | ||||||
chr14:49677335
|
T | C | 55 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(52): Show | 56 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.245+2390A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677335 | ||||||
chr14:49677535
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0212 | 2 | NA18961.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.245+2190C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677535 | ||||||
chr14:49677547
|
G | A | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.245+2178C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677547 | ||||||
chr14:49677615
|
G | A | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+2110C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677615 | ||||||
chr14:49677755
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.245+1970C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677755 | ||||||
chr14:49677927
|
T | C | 2 | a0002c0006t0002g0005a0002c0008t0002g0227 | 2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.245+1798A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677927 | ||||||
chr14:49677980
|
CTTTATTT others(7): Show |
C | 2 | a0001c0001t0001g0145a0001c0001t0002g0065 | 2 | HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.245+1731_245+1744d others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677980 | ||||||
chr14:49677998
|
AT | A | 30 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0033others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.245+1726delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677998 | ||||||
chr14:49678000
|
TTTA | T | 21 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(18): Show | 22 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.245+1722_245+1724d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678000 | ||||||
chr14:49678002
|
T | A | 12 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0002g0030others(9): Show | 12 | HG01361.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.245+1723A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678002 | ||||||
chr14:49678003
|
A | T | 13 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0002g0030others(10): Show | 13 | HG01361.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.245+1722T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678003 | ||||||
chr14:49678005
|
T | A | 20 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(17): Show | 21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.245+1720A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678005 | ||||||
chr14:49678007
|
T | A | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+1718A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678007 | ||||||
chr14:49678063
|
G | A | 3 | a0001c0002t0002g0162a0003c0005t0002g0006a0003c0005t0002g0007 | 3 | HG00597.hp1 HG02055.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.245+1662C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678063 | ||||||
chr14:49678133
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.245+1592C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678133 | ||||||
chr14:49678294
|
C | T | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.245+1431G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678294 | ||||||
chr14:49678339
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+1386C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678339 | ||||||
chr14:49678397
|
C | G | 21 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(18): Show | 22 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.245+1328G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678397 | ||||||
chr14:49678409
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.245+1316A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678409 | ||||||
chr14:49678410
|
G | T | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.245+1315C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678410 | ||||||
chr14:49678488
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.245+1237A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678488 | ||||||
chr14:49678619
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.245+1106A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678619 | ||||||
chr14:49678703
|
C | T | 3 | a0001c0003t0002g0209a0001c0003t0002g0213a0005c0007t0002g0161 | 3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.245+1022G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678703 | ||||||
chr14:49678803
|
C | T | 20 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(17): Show | 21 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.245+922G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678803 | ||||||
chr14:49678846
|
T | TG | 61 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(58): Show | 62 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.245+878dupC | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678846 | ||||||
chr14:49678953
|
G | A | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.245+772C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678953 | ||||||
chr14:49678963
|
T | C | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+762A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678963 | ||||||
chr14:49679186
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0165 | 3 | NA18979.hp2 NA19000.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.245+539G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679186 | ||||||
chr14:49679190
|
CA | C | 18 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(15): Show | 19 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.245+534delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679190 | ||||||
chr14:49679413
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245+312T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679413 | ||||||
chr14:49679425
|
A | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.245+300T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679425 | ||||||
chr14:49679470
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.245+255C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679470 | ||||||
chr14:49679680
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.245+45G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679680 | ||||||
chr14:49679806
|
A | G | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.170-6T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679806 | ||||||
chr14:49679835
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.170-35G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679835 | ||||||
chr14:49679835
|
C | CA | 21 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(18): Show | 22 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.170-36dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679835 | ||||||
chr14:49679839
|
A | C | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.170-39T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679839 | ||||||
chr14:49680003
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.170-203T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680003 | ||||||
chr14:49680142
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.170-342C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680142 | ||||||
chr14:49680353
|
C | CA | 67 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0201others(64): Show | 68 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.170-554dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680353 | ||||||
chr14:49680639
|
GA | G | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-840delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680639 | ||||||
chr14:49680690
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.170-890C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680690 | ||||||
chr14:49680822
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.170-1022C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680822 | ||||||
chr14:49680852
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.170-1052G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680852 | ||||||
chr14:49680900
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.170-1100G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680900 | ||||||
chr14:49681140
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.170-1340A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681140 | ||||||
chr14:49681156
|
C | T | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-1356G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681156 | ||||||
chr14:49681260
|
C | A | 3 | a0001c0004t0004g0086a0003c0005t0002g0006a0003c0005t0002g0007 | 3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.170-1460G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681260 | ||||||
chr14:49681458
|
C | A | 3 | a0001c0004t0004g0086a0003c0005t0002g0006a0003c0005t0002g0007 | 3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.170-1658G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681458 | ||||||
chr14:49681526
|
C | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.170-1726G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681526 | ||||||
chr14:49681723
|
AAGATGGC others(17): Show |
A | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169+1846_169+1869d others(26): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681723 | ||||||
chr14:49681730
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.169+1863G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681730 | ||||||
chr14:49681755
|
G | A | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169+1838C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681755 | ||||||
chr14:49681776
|
G | A | 1 | a0001c0002t0002g0226 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.169+1817C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681776 | ||||||
chr14:49681830
|
C | CA | 8 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0204others(5): Show | 8 | HG00642.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+1762dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681830 | ||||||
chr14:49681830
|
CA | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0098others(5): Show | 9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+1762delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681830 | ||||||
chr14:49681878
|
C | G | 3 | a0001c0004t0004g0086a0003c0005t0002g0006a0003c0005t0002g0007 | 3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.169+1715G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681878 | ||||||
chr14:49681951
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0063others(1): Show | 4 | HG01433.hp1 HG01884.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1642T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681951 | ||||||
chr14:49682004
|
C | CT | 7 | a0001c0001t0001g0020a0001c0001t0001g0078a0001c0001t0001g0094others(4): Show | 7 | HG00741.hp2 HG01099.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+1588dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682004 | ||||||
chr14:49682004
|
CT | C | 5 | a0001c0002t0002g0162a0001c0002t0002g0221a0001c0003t0002g0209others(2): Show | 5 | HG01943.hp2 HG02055.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+1588delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682004 | ||||||
chr14:49682161
|
T | C | 16 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(13): Show | 17 | HG01099.hp1 HG01358.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+1432A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682161 | ||||||
chr14:49682367
|
A | G | 63 | a0001c0001t0001g0037a0001c0001t0001g0082a0001c0001t0001g0083others(60): Show | 64 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.169+1226T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682367 | ||||||
chr14:49682443
|
C | T | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1150G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682443 | ||||||
chr14:49682530
|
G | A | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1063C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682530 | ||||||
chr14:49682569
|
A | G | 53 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(50): Show | 54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+1024T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682569 | ||||||
chr14:49682572
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1021C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682572 | ||||||
chr14:49682573
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1020C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682573 | ||||||
chr14:49682576
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1017C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682576 | ||||||
chr14:49682577
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1016G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682577 | ||||||
chr14:49682578
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1015T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682578 | ||||||
chr14:49682579
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1014C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682579 | ||||||
chr14:49682581
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1012C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682581 | ||||||
chr14:49682582
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1011T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682582 | ||||||
chr14:49682583
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1010C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682583 | ||||||
chr14:49682584
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1009G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682584 | ||||||
chr14:49682586
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1007C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682586 | ||||||
chr14:49682588
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1005T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682588 | ||||||
chr14:49682589
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1003_169+1004i others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682589 | ||||||
chr14:49682591
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1002T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682591 | ||||||
chr14:49682599
|
T | G | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+994A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682599 | ||||||
chr14:49682600
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+993C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682600 | ||||||
chr14:49682601
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+992G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682601 | ||||||
chr14:49682615
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169+978G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682615 | ||||||
chr14:49682640
|
G | GA | 45 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0063others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.169+952dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(7): Show |
1 | a0001c0002t0002g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.169+939_169+952dup others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(8): Show |
4 | a0001c0002t0002g0030a0001c0002t0002g0158a0001c0002t0002g0206others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+938_169+952dup others(15): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(9): Show |
4 | a0001c0002t0002g0031a0001c0002t0002g0075a0001c0002t0002g0159others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+937_169+952dup others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(10): Show |
2 | a0001c0002t0002g0174a0001c0002t0002g0175 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.169+936_169+952dup others(17): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(11): Show |
2 | a0001c0002t0002g0176a0004c0009t0002g0228 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169+935_169+952dup others(18): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(12): Show |
1 | a0001c0002t0002g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+934_169+952dup others(19): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GAAAAAAA others(14): Show |
1 | a0001c0002t0002g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+932_169+952dup others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GGAAAAAA others(5): Show |
1 | a0001c0002t0002g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.169+952_169+953ins others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
G | GGAAAAAA others(9): Show |
1 | a0001c0002t0002g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169+952_169+953ins others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
GA | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0097a0001c0002t0002g0216others(7): Show | 10 | HG01167.hp2 HG01515.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+952delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
GAAA | G | 14 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(11): Show | 15 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+950_169+952del others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682640
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169+942_169+952del others(11): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | ||||||
chr14:49682644
|
A | G | 14 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(11): Show | 15 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+949T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682644 | ||||||
chr14:49682645
|
A | G | 14 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(11): Show | 15 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+948T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682645 | ||||||
chr14:49682691
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+902T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682691 | ||||||
chr14:49682694
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0096 | 2 | HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.169+899T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682694 | ||||||
chr14:49682723
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+870A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682723 | ||||||
chr14:49682725
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+868T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682725 | ||||||
chr14:49682727
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+866A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682727 | ||||||
chr14:49682749
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+844G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682749 | ||||||
chr14:49682826
|
TA | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0094others(17): Show | 21 | HG01099.hp1 HG01099.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+766delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682826 | ||||||
chr14:49682843
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.169+750A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682843 | ||||||
chr14:49682873
|
T | C | 3 | a0001c0004t0004g0086a0003c0005t0002g0006a0003c0005t0002g0007 | 3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.169+720A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682873 | ||||||
chr14:49682965
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+628G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682965 | ||||||
chr14:49682988
|
G | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+605C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682988 | ||||||
chr14:49682989
|
A | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+604T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682989 | ||||||
chr14:49682990
|
A | AAATTGGG others(166): Show |
2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+602_169+603ins others(173): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682990 | ||||||
chr14:49682991
|
G | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+602C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682991 | ||||||
chr14:49682992
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+601G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682992 | ||||||
chr14:49683009
|
G | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG00280.hp1 HG00642.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.169+584C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49683009 | ||||||
chr14:49683030
|
G | A | 4 | a0001c0003t0002g0209a0001c0003t0002g0213a0001c0004t0004g0160others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+563C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49683030 | ||||||
chr14:49683305
|
G | A | 1 | a0001c0002t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+288C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49683305 | ||||||
chr14:49683803
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.69-110G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49683803 | ||||||
chr14:49683859
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.69-166A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49683859 | ||||||
chr14:49683999
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69-306T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49683999 | ||||||
chr14:49684234
|
G | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.69-541C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684234 | ||||||
chr14:49684373
|
G | A | 29 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.69-680C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684373 | ||||||
chr14:49684410
|
A | C | 29 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.69-717T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684410 | ||||||
chr14:49684422
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG00642.hp1 HG01168.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-729C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684422 | ||||||
chr14:49684473
|
A | G | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.69-780T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684473 | ||||||
chr14:49684490
|
T | G | 34 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0033others(31): Show | 34 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.69-797A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684490 | ||||||
chr14:49684623
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69-930T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684623 | ||||||
chr14:49684661
|
T | TA | 19 | a0001c0001t0001g0032a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.69-969dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684661 | ||||||
chr14:49684661
|
TA | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0089others(7): Show | 10 | HG00558.hp1 HG01099.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-969delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684661 | ||||||
chr14:49684745
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.69-1052C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684745 | ||||||
chr14:49684765
|
A | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.69-1072T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684765 | ||||||
chr14:49685657
|
T | C | 1 | a0001c0002t0002g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69-1964A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685657 | ||||||
chr14:49685715
|
T | A | 1 | a0001c0002t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.69-2022A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685715 | ||||||
chr14:49685789
|
G | GTTTT | 19 | a0001c0001t0001g0037a0001c0002t0001g0002a0001c0002t0001g0010others(16): Show | 20 | HG00597.hp1 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.69-2100_69-2097dup others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685789 | ||||||
chr14:49685790
|
T | G | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.69-2097A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685790 | ||||||
chr14:49685876
|
C | T | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69-2183G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685876 | ||||||
chr14:49685897
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.69-2204C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685897 | ||||||
chr14:49685964
|
CT | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02622.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.68+2171delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685964 | ||||||
chr14:49686017
|
C | T | 1 | a0001c0002t0002g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.68+2119G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686017 | ||||||
chr14:49686043
|
C | T | 3 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0012 | 3 | HG02809.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68+2093G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686043 | ||||||
chr14:49686448
|
A | G | 1 | a0001c0002t0002g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.68+1688T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686448 | ||||||
chr14:49686471
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.68+1665T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686471 | ||||||
chr14:49686501
|
A | G | 1 | a0001c0004t0004g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.68+1635T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686501 | ||||||
chr14:49686526
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.68+1610C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686526 | ||||||
chr14:49686543
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.68+1593T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686543 | ||||||
chr14:49686855
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68+1281G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686855 | ||||||
chr14:49686871
|
GCA | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02622.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.68+1263_68+1264del others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686871 | ||||||
chr14:49686983
|
T | A | 1 | a0004c0009t0002g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.68+1153A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686983 | ||||||
chr14:49686985
|
T | C | 6 | a0001c0002t0002g0033a0001c0002t0002g0174a0001c0002t0002g0175others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+1151A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686985 | ||||||
chr14:49687158
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68+978C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687158 | ||||||
chr14:49687191
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.68+945C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687191 | ||||||
chr14:49687257
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.68+879A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687257 | ||||||
chr14:49687278
|
C | CAT | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00438.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68+856_68+857dupAT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687278 | ||||||
chr14:49687292
|
C | T | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+844G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687292 | ||||||
chr14:49687295
|
ACACAC | A | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+836_68+840delGT others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687295 | ||||||
chr14:49687300
|
C | CCA | 30 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0189others(27): Show | 30 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.68+834_68+835dupTG | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687300
|
C | CCACA | 3 | a0001c0001t0001g0212a0001c0001t0002g0211a0001c0003t0002g0213 | 3 | HG01258.hp2 HG02970.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.68+832_68+835dupTG others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687300
|
C | CCACACA | 11 | a0001c0001t0001g0214a0001c0002t0002g0216a0001c0002t0002g0217others(8): Show | 11 | HG00735.hp1 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+830_68+835dupTG others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687300
|
C | CCACACAC others(1): Show |
4 | a0001c0002t0002g0223a0001c0002t0002g0225a0001c0002t0002g0226others(1): Show | 4 | HG01515.hp2 HG01978.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+828_68+835dupTG others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687300
|
CCA | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0037others(44): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.68+834_68+835delTG | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687300
|
CCACA | C | 25 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG01361.hp2 HG01981.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.68+832_68+835delTG others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687300
|
CCACACAC others(9): Show |
C | 2 | a0001c0003t0002g0008a0001c0003t0002g0009 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.68+820_68+835delTG others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | ||||||
chr14:49687307
|
CA | C | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+828delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687307 | ||||||
chr14:49687572
|
G | C | 1 | a0002c0008t0002g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68+564C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687572 | ||||||
chr14:49687727
|
GTCTC | G | 2 | a0003c0005t0002g0006a0003c0005t0002g0007 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+405_68+408delGA others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687727 |