Item | Value |
---|---|
geneid | 2071 |
ensemblid | ENSG00000163161.14 |
hgncid | 3435 |
symbol | ERCC3 |
name | ERCC excision repair 3, TFIIH core complex helicase subunit |
refseq_nuc | NM_000122.2 |
refseq_prot | NP_000113.1 |
ensembl_nuc | ENST00000285398.7 |
ensembl_prot | ENSP00000285398.2 |
mane_status | MANE Select |
chr | chr2 |
start | 127257290 |
end | 127294144 |
strand | - |
ver | v1.2 |
region | chr2:127257290-127294144 |
region5000 | chr2:127252290-127299144 |
regionname0 | ERCC3_chr2_127257290_127294144 |
regionname5000 | ERCC3_chr2_127252290_127299144 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 782 | 346 | 91 | 69 | 131 | 8 | 45 | 101 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0002 | 0/0 | 782 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0003 | 0/0 | 782 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0004 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0005 | 0/0 | 782 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2349 | 329 | 78 | 67 | 130 | 8 | 44 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0002 | 0/0 | 2349 | 6 | 5 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0003 | 0/0 | 2349 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0004 | 0/0 | 2349 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0005 | 0/0 | 2349 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0006 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0007 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0008 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0009 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0010 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
c0011 | 0/0 | 2349 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 370 | 335 | 86 | 63 | 130 | 8 | 46 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
t0002 | 0/0 | 370 | 6 | 5 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
t0003 | 0/0 | 370 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
t0004 | 0/0 | 370 | 3 | 1 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
t0005 | 0/0 | 370 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 20 | 3 | 5 | 11 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0002 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0003 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0004 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0011 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2349 | 329 | 78 | 67 | 130 | 8 | 44 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0001c0002 | 0/0 | 2349 | 6 | 5 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0001c0003 | 0/0 | 2349 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0001c0004 | 0/0 | 2349 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0001c0005 | 0/0 | 2349 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0001c0008 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0001c0010 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0002c0009 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0003c0007 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0004c0006 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 | |
a0005c0011 | 0/0 | 2349 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2718 | 315 | 73 | 60 | 128 | 8 | 44 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0001t0002 | 0/0 | 2718 | 5 | 4 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0001t0003 | 0/0 | 2718 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0001t0004 | 0/0 | 2718 | 3 | 1 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0001t0005 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0002t0001 | 0/0 | 2718 | 6 | 5 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0003t0001 | 0/0 | 2718 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0004t0001 | 0/0 | 2718 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0005t0001 | 0/0 | 2718 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0008t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0001c0010t0001 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0002c0009t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0003c0007t0001 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0004c0006t0002 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
a0005c0011t0001 | 0/0 | 2718 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | copy fasta | chr2 | 127252290 | 127299144 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 3 | 5 | 11 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0003 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0002t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0003t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0004t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0004t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0001c0010t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0002c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0003c0007t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0004c0006t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
a0005c0011t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0234 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0220 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01975 | hp2 | a0005 | c0011 | t0001 | g0235 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0042 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0225 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02738 | hp1 | a0001 | c0010 | t0001 | g0258 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0222 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0224 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03209 | hp1 | a0004 | c0006 | t0002 | g0261 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18991 | hp2 | a0002 | c0009 | t0001 | g0229 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19075 | hp1 | a0001 | c0008 | t0001 | g0092 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20905 | hp1 | a0003 | c0007 | t0001 | g0179 | SAS | GIH | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127259310 | A | G | 1 | a0002 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.2203T>C | p.Ser735Pro | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/15 | 2266/2718 | 2203/2349 | 735/782 | chr2 | 127259310 | ||
chr2:127261332 | C | T | 1 | a0003 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1960G>A | p.Glu654Lys | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/15 | 2023/2718 | 1960/2349 | 654/782 | chr2 | 127261332 | ||
chr2:127286997 | C | T | 1 | a0004 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1048G>A | p.Gly350Ser | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/15 | 1111/2718 | 1048/2349 | 350/782 | chr2 | 127286997 | ||
chr2:127292833 | T | C | 1 | a0005 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.248A>G | p.His83Arg | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/15 | 311/2718 | 248/2349 | 83/782 | chr2 | 127292833 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127259407 | C | T | 1 | a0001c0008 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.2106G>A | p.Ala702Ala | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/15 | 2169/2718 | 2106/2349 | 702/782 | chr2 | 127259407 | ||
chr2:127280489 | C | T | 1 | a0001c0002 | 6 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.1485G>A | p.Glu495Glu | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/15 | 1548/2718 | 1485/2349 | 495/782 | chr2 | 127280489 | ||
chr2:127286926 | C | T | 1 | a0001c0003 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.1119G>A | p.Gln373Gln | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/15 | 1182/2718 | 1119/2349 | 373/782 | chr2 | 127286926 | ||
chr2:127288679 | C | T | 1 | a0001c0005 | 2 | HG02622.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1008G>A | p.Gly336Gly | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/15 | 1071/2718 | 1008/2349 | 336/782 | chr2 | 127288679 | ||
chr2:127289731 | C | T | 1 | a0001c0004 | 3 | HG01175.hp1 HG02257.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.615G>A | p.Glu205Glu | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 5/15 | 678/2718 | 615/2349 | 205/782 | chr2 | 127289731 | ||
chr2:127289818 | G | A | 1 | a0001c0010 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.528C>T | p.Phe176Phe | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 5/15 | 591/2718 | 528/2349 | 176/782 | chr2 | 127289818 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127257337 | C | T | 1 | a0001c0001t0004 | 3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*259G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 15/15 | 259 | chr2 | 127257337 | |||||
chr2:127257419 | T | C | 1 | a0001c0001t0003 | 4 | HG01099.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 15/15 | 177 | chr2 | 127257419 | |||||
chr2:127257490 | A | G | 2 | a0001c0001t0002a0004c0006t0002 | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 15/15 | 106 | chr2 | 127257490 | |||||
chr2:127294132 | C | T | 1 | a0001c0001t0005 | 2 | HG02083.hp1 HG02523.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/15 | 51 | chr2 | 127294132 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127257733 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.2218-6C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257733 | ||||||
chr2:127257791 | C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 302 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.2218-64G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257791 | ||||||
chr2:127257818 | C | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0083others(5): Show | 11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2218-91G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257818 | ||||||
chr2:127257843 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2218-116A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257843 | ||||||
chr2:127258104 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2218-377A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258104 | ||||||
chr2:127258179 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2218-452G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258179 | ||||||
chr2:127258224 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2218-497A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258224 | ||||||
chr2:127258268 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2218-541G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258268 | ||||||
chr2:127258415 | G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2218-688C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258415 | ||||||
chr2:127258631 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+665C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258631 | ||||||
chr2:127258658 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2217+638C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258658 | ||||||
chr2:127258827 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+469C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258827 | ||||||
chr2:127258852 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2217+444T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258852 | ||||||
chr2:127258988 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+308T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258988 | ||||||
chr2:127259085 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+211C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127259085 | ||||||
chr2:127259166 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2217+130G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127259166 | ||||||
chr2:127259608 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2065-160C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259608 | ||||||
chr2:127259715 | T | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2065-267A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259715 | ||||||
chr2:127259764 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2065-316G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259764 | ||||||
chr2:127259764 | C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2065-316G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259764 | ||||||
chr2:127259806 | G | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-358C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259806 | ||||||
chr2:127259915 | A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0216a0001c0001t0001g0217 | 5 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-467T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259915 | ||||||
chr2:127260190 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2065-742C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260190 | ||||||
chr2:127260208 | C | T | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2065-760G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260208 | ||||||
chr2:127260487 | A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2064+741T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260487 | ||||||
chr2:127260517 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2064+711C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260517 | ||||||
chr2:127260566 | T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0126 | 4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+662A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260566 | ||||||
chr2:127260616 | A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(101): Show | 138 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.2064+612T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260616 | ||||||
chr2:127260884 | GGAGGCAA others(3): Show |
G | 18 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(15): Show | 19 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2064+334_2064+343d others(12): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260884 | ||||||
chr2:127260946 | T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.2064+282A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260946 | ||||||
chr2:127260985 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2064+243C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260985 | ||||||
chr2:127261169 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2064+59C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127261169 | ||||||
chr2:127261367 | C | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1946-21G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261367 | ||||||
chr2:127261416 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-70A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261416 | ||||||
chr2:127261486 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1946-140C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261486 | ||||||
chr2:127261602 | G | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1946-256C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261602 | ||||||
chr2:127261665 | A | C | 1 | a0001c0001t0001g0022 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1946-319T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261665 | ||||||
chr2:127261879 | G | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-533C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261879 | ||||||
chr2:127262083 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1946-737G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262083 | ||||||
chr2:127262139 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1946-793A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262139 | ||||||
chr2:127262425 | A | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-1079T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262425 | ||||||
chr2:127262775 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-1429C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262775 | ||||||
chr2:127262791 | G | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0075a0001c0001t0001g0095others(4): Show | 8 | HG02165.hp1 NA18945.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1946-1445C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262791 | ||||||
chr2:127262798 | C | T | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1946-1452G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262798 | ||||||
chr2:127262970 | G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 89 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1946-1624C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262970 | ||||||
chr2:127263092 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1946-1746A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263092 | ||||||
chr2:127263181 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1946-1835A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263181 | ||||||
chr2:127263366 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1946-2020C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263366 | ||||||
chr2:127263480 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-2134G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263480 | ||||||
chr2:127263666 | T | C | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01256.hp1 HG01358.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1946-2320A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263666 | ||||||
chr2:127263702 | GTTCT | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 99 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1946-2360_1946-235 others(8): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263702 | ||||||
chr2:127263738 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1946-2392G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263738 | ||||||
chr2:127263776 | C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-2430G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263776 | ||||||
chr2:127263828 | C | T | 19 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(16): Show | 20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1946-2482G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263828 | ||||||
chr2:127263868 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1946-2522G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263868 | ||||||
chr2:127263978 | C | T | 22 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(19): Show | 24 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1946-2632G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263978 | ||||||
chr2:127264053 | A | G | 23 | a0001c0001t0001g0047a0001c0001t0001g0211a0001c0001t0001g0212others(20): Show | 25 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1946-2707T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264053 | ||||||
chr2:127264143 | T | C | 1 | a0001c0005t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1946-2797A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264143 | ||||||
chr2:127264189 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1946-2843G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264189 | ||||||
chr2:127264216 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-2870G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264216 | ||||||
chr2:127264318 | T | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0083others(5): Show | 11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1946-2972A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264318 | ||||||
chr2:127264517 | T | C | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1946-3171A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264517 | ||||||
chr2:127264528 | T | C | 1 | a0001c0001t0001g0012 | 3 | HG02451.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1946-3182A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264528 | ||||||
chr2:127264539 | T | A | 1 | a0001c0001t0001g0030 | 2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1946-3193A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264539 | ||||||
chr2:127264639 | C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1946-3293G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264639 | ||||||
chr2:127264708 | T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-3362A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264708 | ||||||
chr2:127264847 | A | AT | 13 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0071others(10): Show | 14 | HG01175.hp1 HG01192.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1946-3502dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264847 | ||||||
chr2:127264847 | AT | A | 6 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0001t0001g0108others(3): Show | 6 | HG01256.hp1 HG01358.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1946-3502delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264847 | ||||||
chr2:127264871 | G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0252 | 2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1946-3525C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264871 | ||||||
chr2:127265095 | C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1946-3749G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265095 | ||||||
chr2:127265189 | G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0214others(11): Show | 17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1946-3843C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265189 | ||||||
chr2:127265192 | C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0126 | 4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1946-3846G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265192 | ||||||
chr2:127265320 | G | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0249 | 2 | NA18970.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1946-3974C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265320 | ||||||
chr2:127265465 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1946-4119G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265465 | ||||||
chr2:127265519 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1946-4173G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265519 | ||||||
chr2:127265519 | C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0123others(1): Show | 5 | HG02647.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1946-4173G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265519 | ||||||
chr2:127265680 | G | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1946-4334C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265680 | ||||||
chr2:127265741 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1946-4395G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265741 | ||||||
chr2:127265766 | T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG01884.hp1 HG01891.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1946-4420A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265766 | ||||||
chr2:127265773 | T | C | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1946-4427A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265773 | ||||||
chr2:127265947 | C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0057others(3): Show | 7 | HG00741.hp1 HG01106.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1946-4601G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265947 | ||||||
chr2:127266082 | G | GT | 11 | a0001c0001t0001g0100a0001c0001t0001g0164a0001c0001t0001g0182others(8): Show | 11 | HG01256.hp1 HG01358.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1946-4737dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266082 | ||||||
chr2:127266085 | T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-4739A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266085 | ||||||
chr2:127266112 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1946-4766G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266112 | ||||||
chr2:127266196 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-4850G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266196 | ||||||
chr2:127266287 | C | CAAGAAAA others(326): Show |
1 | a0001c0001t0001g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1946-4942_1946-494 others(337): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266287 | ||||||
chr2:127266287 | C | CAAGAAAA others(327): Show |
3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG03041.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1946-4942_1946-494 others(338): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266287 | ||||||
chr2:127266308 | T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1946-4962A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266308 | ||||||
chr2:127266333 | C | CT | 50 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 61 | HG00423.hp1 HG00735.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1946-4988dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266333 | ||||||
chr2:127266333 | C | CTT | 12 | a0001c0001t0001g0012a0001c0001t0001g0218a0001c0001t0001g0240others(9): Show | 15 | HG00423.hp2 HG01069.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1946-4989_1946-498 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266333 | ||||||
chr2:127266333 | CTTTTTTT others(1): Show |
C | 94 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(91): Show | 126 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1945+4995_1946-498 others(12): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266333 | ||||||
chr2:127266354 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4982A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266354 | ||||||
chr2:127266355 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4981A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266355 | ||||||
chr2:127266358 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4978C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266358 | ||||||
chr2:127266362 | G | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1945+4974C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266362 | ||||||
chr2:127266367 | G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1945+4969C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266367 | ||||||
chr2:127266374 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1945+4962A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266374 | ||||||
chr2:127266398 | C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0222a0001c0003t0001g0226 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+4938G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266398 | ||||||
chr2:127266549 | G | A | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0259 | 3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1945+4787C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266549 | ||||||
chr2:127266559 | G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0158 | 2 | NA18939.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1945+4777C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266559 | ||||||
chr2:127266587 | T | C | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945+4749A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266587 | ||||||
chr2:127266603 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1945+4733G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266603 | ||||||
chr2:127266605 | G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0026 | 4 | HG00733.hp2 HG01070.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+4731C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266605 | ||||||
chr2:127266621 | G | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+4715C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266621 | ||||||
chr2:127266650 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1945+4686G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266650 | ||||||
chr2:127266663 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1945+4673C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266663 | ||||||
chr2:127266706 | ATTATTTT others(4): Show |
A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4619_1945+462 others(15): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266706 | ||||||
chr2:127266709 | A | AT | 66 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 81 | HG00423.hp1 HG00642.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1945+4626dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266709 | A | ATT | 16 | a0001c0001t0001g0172a0001c0001t0001g0228a0001c0001t0001g0230others(13): Show | 16 | HG00423.hp2 HG01243.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1945+4625_1945+462 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266709 | A | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG04184.hp2 HG06807.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+4627T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266709 | AT | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0107others(3): Show | 7 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1945+4626delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266709 | ATT | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0114others(3): Show | 8 | NA18951.hp2 NA18953.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1945+4625_1945+462 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266709 | ATTTTTTT | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0173a0001c0001t0001g0183others(1): Show | 6 | HG01433.hp2 HG02698.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945+4620_1945+462 others(11): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266709 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1945+4616_1945+462 others(15): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | ||||||
chr2:127266717 | T | TA | 3 | a0001c0001t0001g0010a0001c0001t0001g0216a0001c0001t0001g0217 | 5 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+4618_1945+461 others(5): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266717 | ||||||
chr2:127266841 | C | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+4495G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266841 | ||||||
chr2:127266868 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1945+4468G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266868 | ||||||
chr2:127266869 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1945+4467C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266869 | ||||||
chr2:127266881 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1945+4455A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266881 | ||||||
chr2:127266904 | C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0256 | 2 | HG03516.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1945+4432G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266904 | ||||||
chr2:127266915 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1945+4421G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266915 | ||||||
chr2:127266969 | G | A | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945+4367C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266969 | ||||||
chr2:127267194 | T | C | 1 | a0001c0005t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1945+4142A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267194 | ||||||
chr2:127267288 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1945+4048G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267288 | ||||||
chr2:127267323 | G | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+4013C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267323 | ||||||
chr2:127267376 | C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1945+3960G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267376 | ||||||
chr2:127267429 | C | CT | 4 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0216others(1): Show | 6 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945+3906dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267429 | ||||||
chr2:127267453 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1945+3883A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267453 | ||||||
chr2:127267829 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1945+3507A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267829 | ||||||
chr2:127267857 | A | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0222a0001c0003t0001g0226 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+3479T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267857 | ||||||
chr2:127267950 | T | C | 1 | a0001c0001t0004g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1945+3386A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267950 | ||||||
chr2:127268023 | G | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+3313C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268023 | ||||||
chr2:127268076 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3260G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268076 | ||||||
chr2:127268118 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3218A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268118 | ||||||
chr2:127268173 | G | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1945+3163C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268173 | ||||||
chr2:127268255 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3081C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268255 | ||||||
chr2:127268262 | T | C | 2 | a0001c0001t0002g0263a0001c0001t0002g0264 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1945+3074A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268262 | ||||||
chr2:127268285 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3051T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268285 | ||||||
chr2:127268295 | G | T | 1 | a0001c0001t0001g0195 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1945+3041C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268295 | ||||||
chr2:127268368 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+2968G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268368 | ||||||
chr2:127268509 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1945+2827A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268509 | ||||||
chr2:127268549 | C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1945+2787G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268549 | ||||||
chr2:127268550 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1945+2786C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268550 | ||||||
chr2:127268850 | C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1945+2486G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268850 | ||||||
chr2:127268984 | TG | T | 18 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(15): Show | 19 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1945+2351delC | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268984 | ||||||
chr2:127269098 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1945+2238A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269098 | ||||||
chr2:127269209 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+2127T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269209 | ||||||
chr2:127269335 | T | A | 4 | a0001c0001t0001g0223a0001c0003t0001g0040a0001c0003t0001g0222others(1): Show | 5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+2001A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269335 | ||||||
chr2:127269417 | C | CT | 25 | a0001c0001t0001g0017a0001c0001t0001g0057a0001c0001t0001g0058others(22): Show | 27 | HG01069.hp2 HG01109.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1945+1918dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269417 | ||||||
chr2:127269417 | CT | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 109 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1945+1918delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269417 | ||||||
chr2:127269482 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1945+1854G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269482 | ||||||
chr2:127269522 | C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0241a0001c0001t0001g0247others(1): Show | 8 | HG01346.hp1 HG02683.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1945+1814G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269522 | ||||||
chr2:127269657 | A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0187 | 2 | HG01074.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1945+1679T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269657 | ||||||
chr2:127269672 | G | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1945+1664C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269672 | ||||||
chr2:127269706 | C | A | 6 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG01256.hp1 HG01358.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945+1630G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269706 | ||||||
chr2:127269711 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1945+1625C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269711 | ||||||
chr2:127269756 | C | A | 12 | a0001c0001t0001g0228a0001c0001t0001g0265a0001c0001t0001g0266others(9): Show | 13 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1945+1580G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269756 | ||||||
chr2:127269904 | G | C | 19 | a0001c0001t0001g0047a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1945+1432C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269904 | ||||||
chr2:127270018 | C | CTCAA | 80 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 111 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1945+1314_1945+131 others(8): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270018 | ||||||
chr2:127270018 | C | CTCAATCA others(1): Show |
4 | a0001c0001t0001g0032a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 5 | HG01261.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+1310_1945+131 others(12): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270018 | ||||||
chr2:127270018 | C | CTCAATCA others(5): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1945+1306_1945+131 others(16): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270018 | ||||||
chr2:127270048 | A | C | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945+1288T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270048 | ||||||
chr2:127270049 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1945+1287T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270049 | ||||||
chr2:127270075 | A | G | 1 | a0001c0004t0001g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1945+1261T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270075 | ||||||
chr2:127270173 | A | ACACACCA others(10): Show |
3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1945+1146_1945+116 others(21): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270173 | ||||||
chr2:127270197 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1945+1139A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270197 | ||||||
chr2:127270276 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+1060A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270276 | ||||||
chr2:127270304 | T | C | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+1032A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270304 | ||||||
chr2:127270554 | G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 129 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1945+782C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270554 | ||||||
chr2:127270906 | G | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+430C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270906 | ||||||
chr2:127270919 | G | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+417C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270919 | ||||||
chr2:127270962 | T | A | 1 | a0001c0005t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1945+374A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270962 | ||||||
chr2:127271216 | T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1945+120A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127271216 | ||||||
chr2:127271489 | GA | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 140 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1828-37delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271489 | ||||||
chr2:127271689 | C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0216a0001c0001t0001g0217 | 5 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1828-236G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271689 | ||||||
chr2:127271732 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-279C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271732 | ||||||
chr2:127271927 | C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1828-474G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271927 | ||||||
chr2:127271938 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-485C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271938 | ||||||
chr2:127271983 | C | A | 1 | a0002c0009t0001g0229 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1828-530G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271983 | ||||||
chr2:127272007 | C | CT | 15 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0048others(12): Show | 17 | HG00741.hp1 HG01106.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1828-555dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | ||||||
chr2:127272007 | CT | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(146): Show | 204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1828-555delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | ||||||
chr2:127272007 | CTT | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 46 | HG00639.hp1 HG01175.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.1828-556_1828-555d others(4): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | ||||||
chr2:127272007 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-567_1828-555d others(15): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | ||||||
chr2:127272007 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0022 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1828-570_1828-555d others(18): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | ||||||
chr2:127272041 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1828-588C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272041 | ||||||
chr2:127272049 | G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1828-596C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272049 | ||||||
chr2:127272101 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1828-648G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272101 | ||||||
chr2:127272109 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-656A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272109 | ||||||
chr2:127272153 | T | C | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828-700A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272153 | ||||||
chr2:127272165 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1827+700G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272165 | ||||||
chr2:127272170 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1827+695C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272170 | ||||||
chr2:127272213 | C | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 85 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1827+652G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272213 | ||||||
chr2:127272259 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1827+606G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272259 | ||||||
chr2:127272262 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1827+603A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272262 | ||||||
chr2:127272272 | G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0083others(5): Show | 11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1827+593C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272272 | ||||||
chr2:127272461 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1827+404G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272461 | ||||||
chr2:127272502 | G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0144others(11): Show | 16 | HG01081.hp1 HG01358.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1827+363C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272502 | ||||||
chr2:127272589 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1827+276T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272589 | ||||||
chr2:127272801 | T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1827+64A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272801 | ||||||
chr2:127272993 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1731-32C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127272993 | ||||||
chr2:127273020 | A | C | 1 | a0001c0001t0001g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1731-59T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273020 | ||||||
chr2:127273109 | T | G | 4 | a0001c0001t0001g0223a0001c0003t0001g0040a0001c0003t0001g0222others(1): Show | 5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-148A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273109 | ||||||
chr2:127273157 | C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0026 | 4 | HG00733.hp2 HG01070.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731-196G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273157 | ||||||
chr2:127273196 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1731-235C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273196 | ||||||
chr2:127273212 | A | C | 4 | a0001c0001t0001g0223a0001c0003t0001g0040a0001c0003t0001g0222others(1): Show | 5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-251T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273212 | ||||||
chr2:127273303 | A | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1731-342T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273303 | ||||||
chr2:127273409 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-448T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273409 | ||||||
chr2:127273475 | C | T | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1731-514G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273475 | ||||||
chr2:127273512 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1731-551A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273512 | ||||||
chr2:127273540 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1731-579C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273540 | ||||||
chr2:127273622 | G | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731-661C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273622 | ||||||
chr2:127273641 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1731-680G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273641 | ||||||
chr2:127273673 | G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 7 | HG01192.hp2 HG01261.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-712C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273673 | ||||||
chr2:127273720 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1731-759G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273720 | ||||||
chr2:127273749 | C | CA | 101 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(98): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1731-789dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | ||||||
chr2:127273749 | C | CAA | 21 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0037others(18): Show | 25 | HG01106.hp2 HG01109.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1731-790_1731-789d others(4): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | ||||||
chr2:127273749 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-800_1731-789d others(14): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | ||||||
chr2:127273749 | CA | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0083others(10): Show | 16 | HG02109.hp2 HG02257.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.1731-789delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | ||||||
chr2:127273749 | CAAAAAA | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0192a0001c0001t0001g0230others(3): Show | 7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-794_1731-789d others(8): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | ||||||
chr2:127273749 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0091 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1731-799_1731-789d others(13): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | ||||||
chr2:127273842 | T | C | 1 | a0001c0010t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1731-881A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273842 | ||||||
chr2:127273962 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1731-1001T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273962 | ||||||
chr2:127274040 | G | A | 6 | a0001c0001t0001g0228a0001c0001t0002g0043a0001c0001t0002g0262others(3): Show | 7 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1079C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274040 | ||||||
chr2:127274079 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-1118C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274079 | ||||||
chr2:127274088 | T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 7 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1127A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274088 | ||||||
chr2:127274123 | G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1731-1162C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274123 | ||||||
chr2:127274222 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1731-1261C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274222 | ||||||
chr2:127274309 | C | T | 14 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(11): Show | 15 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1731-1348G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274309 | ||||||
chr2:127274316 | GA | G | 10 | a0001c0001t0001g0133a0001c0001t0001g0209a0001c0001t0001g0211others(7): Show | 10 | HG01169.hp2 HG01256.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1731-1356delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274316 | ||||||
chr2:127274380 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1731-1419A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274380 | ||||||
chr2:127274441 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1731-1480C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274441 | ||||||
chr2:127274503 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1731-1542G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274503 | ||||||
chr2:127274729 | G | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1731-1768C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274729 | ||||||
chr2:127274754 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-1793G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274754 | ||||||
chr2:127274810 | G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026 | 6 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1731-1849C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274810 | ||||||
chr2:127274820 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-1859G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274820 | ||||||
chr2:127274833 | G | C | 3 | a0001c0001t0003g0039a0001c0001t0003g0206a0001c0001t0003g0207 | 4 | HG01099.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731-1872C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274833 | ||||||
chr2:127274951 | G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0107 | 5 | HG00280.hp1 HG00733.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-1990C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274951 | ||||||
chr2:127274970 | G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1731-2009C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274970 | ||||||
chr2:127275129 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-2168C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275129 | ||||||
chr2:127275246 | A | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1731-2285T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275246 | ||||||
chr2:127275383 | C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0087others(6): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1731-2422G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275383 | ||||||
chr2:127275448 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1731-2487G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275448 | ||||||
chr2:127275559 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-2598T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275559 | ||||||
chr2:127275639 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1731-2678G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275639 | ||||||
chr2:127275751 | C | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 301 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.1731-2790G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275751 | ||||||
chr2:127275829 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-2868C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275829 | ||||||
chr2:127276023 | C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18944.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1731-3062G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276023 | ||||||
chr2:127276156 | C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+3017G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276156 | ||||||
chr2:127276406 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1730+2767T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276406 | ||||||
chr2:127276771 | G | GA | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1730+2401dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276771 | ||||||
chr2:127276845 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1730+2328G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276845 | ||||||
chr2:127276925 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1730+2248T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276925 | ||||||
chr2:127276963 | A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1730+2210T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276963 | ||||||
chr2:127277263 | AGAAATTA others(3): Show |
A | 12 | a0001c0001t0001g0228a0001c0001t0001g0265a0001c0001t0001g0266others(9): Show | 13 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1730+1900_1730+190 others(14): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277263 | ||||||
chr2:127277448 | T | G | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0259 | 3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1730+1725A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277448 | ||||||
chr2:127277517 | C | T | 19 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(16): Show | 20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1730+1656G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277517 | ||||||
chr2:127277521 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1730+1652G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277521 | ||||||
chr2:127277609 | T | G | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+1564A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277609 | ||||||
chr2:127277666 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1730+1507C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277666 | ||||||
chr2:127277749 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1730+1424G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277749 | ||||||
chr2:127277762 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1730+1411G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277762 | ||||||
chr2:127278084 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1730+1089T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278084 | ||||||
chr2:127278238 | C | CA | 7 | a0001c0001t0001g0047a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+934dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278238 | ||||||
chr2:127278238 | CA | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 278 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.1730+934delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278238 | ||||||
chr2:127278272 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1730+901T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278272 | ||||||
chr2:127278307 | C | A | 3 | a0001c0002t0001g0005a0001c0002t0001g0053a0001c0002t0001g0054 | 6 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+866G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278307 | ||||||
chr2:127278307 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1730+866G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278307 | ||||||
chr2:127278388 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1730+785G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278388 | ||||||
chr2:127278575 | G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0083others(5): Show | 11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1730+598C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278575 | ||||||
chr2:127278633 | G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+540C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278633 | ||||||
chr2:127278685 | C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1730+488G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278685 | ||||||
chr2:127278725 | G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0113others(2): Show | 7 | NA18944.hp2 NA18951.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.1730+448C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278725 | ||||||
chr2:127278907 | G | A | 8 | a0001c0001t0001g0228a0001c0001t0002g0043a0001c0001t0002g0262others(5): Show | 9 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1730+266C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278907 | ||||||
chr2:127278911 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1730+262G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278911 | ||||||
chr2:127278912 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1730+261T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278912 | ||||||
chr2:127279095 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1730+78T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127279095 | ||||||
chr2:127279567 | G | T | 8 | a0001c0001t0001g0228a0001c0001t0002g0043a0001c0001t0002g0262others(5): Show | 9 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1528-192C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279567 | ||||||
chr2:127279625 | G | A | 2 | a0001c0001t0004g0220a0001c0001t0004g0221 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1528-250C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279625 | ||||||
chr2:127279670 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1528-295C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279670 | ||||||
chr2:127279759 | T | TA | 7 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0043others(4): Show | 8 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1528-385dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279759 | ||||||
chr2:127279863 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1528-488A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279863 | ||||||
chr2:127279871 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1528-496A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279871 | ||||||
chr2:127279902 | C | T | 23 | a0001c0001t0001g0047a0001c0001t0001g0211a0001c0001t0001g0212others(20): Show | 25 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1528-527G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279902 | ||||||
chr2:127279956 | T | A | 1 | a0001c0001t0001g0012 | 3 | HG02451.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1527+491A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279956 | ||||||
chr2:127279984 | A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1527+463T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279984 | ||||||
chr2:127280178 | C | A | 3 | a0001c0003t0001g0040a0001c0003t0001g0222a0001c0003t0001g0226 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+269G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127280178 | ||||||
chr2:127280328 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1527+119T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127280328 | ||||||
chr2:127280795 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1343-164C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127280795 | ||||||
chr2:127280968 | T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(99): Show | 136 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1343-337A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127280968 | ||||||
chr2:127281077 | G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG00423.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1343-446C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281077 | ||||||
chr2:127281119 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1343-488A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281119 | ||||||
chr2:127281160 | A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0214others(11): Show | 17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1343-529T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281160 | ||||||
chr2:127281162 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-531G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281162 | ||||||
chr2:127281362 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1343-731T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281362 | ||||||
chr2:127281469 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1343-838A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281469 | ||||||
chr2:127281958 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1343-1327T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281958 | ||||||
chr2:127282008 | G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0227 | 3 | HG01069.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1343-1377C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282008 | ||||||
chr2:127282022 | C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0143 | 4 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1343-1391G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282022 | ||||||
chr2:127282123 | C | T | 1 | a0001c0005t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1343-1492G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282123 | ||||||
chr2:127282215 | C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1343-1584G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282215 | ||||||
chr2:127282293 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1343-1662A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282293 | ||||||
chr2:127282386 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1343-1755G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282386 | ||||||
chr2:127282503 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1343-1872T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282503 | ||||||
chr2:127282571 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1343-1940T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282571 | ||||||
chr2:127282615 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-1984C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282615 | ||||||
chr2:127282653 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1343-2022A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282653 | ||||||
chr2:127282687 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1343-2056T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282687 | ||||||
chr2:127282687 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1343-2056T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282687 | ||||||
chr2:127282754 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1343-2123A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282754 | ||||||
chr2:127282795 | C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0222a0001c0003t0001g0226 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343-2164G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282795 | ||||||
chr2:127282909 | G | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0126 | 4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343-2278C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282909 | ||||||
chr2:127283094 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1343-2463A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283094 | ||||||
chr2:127283141 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1343-2510C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283141 | ||||||
chr2:127283143 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1343-2512A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283143 | ||||||
chr2:127283288 | C | T | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1343-2657G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283288 | ||||||
chr2:127283339 | T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(101): Show | 138 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1343-2708A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283339 | ||||||
chr2:127283622 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-2991G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283622 | ||||||
chr2:127283631 | T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1343-3000A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283631 | ||||||
chr2:127283805 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1342+2898T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283805 | ||||||
chr2:127283869 | A | C | 2 | a0001c0001t0005g0045a0001c0001t0005g0046 | 2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1342+2834T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283869 | ||||||
chr2:127283891 | C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0083 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1342+2812G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283891 | ||||||
chr2:127283995 | TGA | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1342+2706_1342+270 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283995 | ||||||
chr2:127284037 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342+2666G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284037 | ||||||
chr2:127284061 | T | C | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1342+2642A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284061 | ||||||
chr2:127284258 | T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0214others(11): Show | 17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1342+2445A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284258 | ||||||
chr2:127284354 | G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1342+2349C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284354 | ||||||
chr2:127284465 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1342+2238C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284465 | ||||||
chr2:127284485 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1342+2218G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284485 | ||||||
chr2:127284524 | C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1342+2179G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284524 | ||||||
chr2:127284533 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1342+2170G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284533 | ||||||
chr2:127284565 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1342+2138T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284565 | ||||||
chr2:127284687 | A | AT | 8 | a0001c0001t0001g0077a0001c0001t0001g0151a0001c0001t0001g0211others(5): Show | 8 | HG01884.hp2 HG02922.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1342+2015dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284687 | ||||||
chr2:127284687 | A | ATT | 25 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(22): Show | 34 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.1342+2014_1342+201 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284687 | ||||||
chr2:127284895 | C | T | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342+1808G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284895 | ||||||
chr2:127284912 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1342+1791G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284912 | ||||||
chr2:127285055 | G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0113others(6): Show | 11 | HG00438.hp1 NA18612.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1342+1648C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285055 | ||||||
chr2:127285056 | C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0222a0001c0003t0001g0226 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1342+1647G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285056 | ||||||
chr2:127285145 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1342+1558C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285145 | ||||||
chr2:127285229 | A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1342+1474T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285229 | ||||||
chr2:127285250 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1342+1453G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285250 | ||||||
chr2:127285296 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1342+1407T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285296 | ||||||
chr2:127285297 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1342+1406G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285297 | ||||||
chr2:127285403 | T | C | 1 | a0001c0005t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1342+1300A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285403 | ||||||
chr2:127285509 | G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0195a0001c0001t0001g0196 | 4 | NA18953.hp2 NA18955.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1342+1194C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285509 | ||||||
chr2:127285573 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1342+1130G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285573 | ||||||
chr2:127285709 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1342+994C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285709 | ||||||
chr2:127285754 | G | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1342+949C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285754 | ||||||
chr2:127285776 | T | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1342+927A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285776 | ||||||
chr2:127285794 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1342+909A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285794 | ||||||
chr2:127285982 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1342+721A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285982 | ||||||
chr2:127285982 | T | TA | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1342+720dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285982 | ||||||
chr2:127286169 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1342+534A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286169 | ||||||
chr2:127286288 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1342+415G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286288 | ||||||
chr2:127286419 | G | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0126 | 4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1342+284C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286419 | ||||||
chr2:127286472 | G | T | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0259 | 3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1342+231C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286472 | ||||||
chr2:127286545 | CA | C | 10 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(7): Show | 10 | HG01081.hp1 HG01358.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1342+157delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286545 | ||||||
chr2:127286617 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1342+86G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286617 | ||||||
chr2:127287354 | A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1028-337T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287354 | ||||||
chr2:127287486 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1028-469A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287486 | ||||||
chr2:127287558 | C | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0121a0001c0001t0001g0122 | 4 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-541G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287558 | ||||||
chr2:127287589 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1028-572C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287589 | ||||||
chr2:127287679 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1028-662A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287679 | ||||||
chr2:127287727 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1028-710G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287727 | ||||||
chr2:127287787 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1028-770C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287787 | ||||||
chr2:127287794 | A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0052 | 4 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-777T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287794 | ||||||
chr2:127287839 | G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1027+821C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287839 | ||||||
chr2:127287847 | G | A | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG03041.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027+813C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287847 | ||||||
chr2:127287912 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1027+748G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287912 | ||||||
chr2:127288391 | C | T | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+269G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127288391 | ||||||
chr2:127288657 | T | C | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1027+3A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127288657 | ||||||
chr2:127288972 | C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(210): Show | 281 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.823-108G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127288972 | ||||||
chr2:127289012 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.823-148T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289012 | ||||||
chr2:127289041 | C | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-177G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289041 | ||||||
chr2:127289062 | T | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02056.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.823-198A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289062 | ||||||
chr2:127289074 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.823-210T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289074 | ||||||
chr2:127289525 | C | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG01261.hp1 HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.658-24G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 5/14 | chr2 | 127289525 | ||||||
chr2:127290044 | G | A | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 10 | HG01099.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.521+180C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290044 | ||||||
chr2:127290066 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.521+158C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290066 | ||||||
chr2:127290094 | TTTCTC | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.521+125_521+129del others(5): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290094 | ||||||
chr2:127290176 | G | A | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.521+48C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290176 | ||||||
chr2:127290181 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.521+43T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290181 | ||||||
chr2:127290372 | C | A | 1 | a0001c0001t0001g0030 | 2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.472-99G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290372 | ||||||
chr2:127290422 | C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0143 | 4 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-149G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290422 | ||||||
chr2:127290473 | C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0222a0001c0003t0001g0226 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-200G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290473 | ||||||
chr2:127290566 | C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 7 | HG01192.hp2 HG01261.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.472-293G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290566 | ||||||
chr2:127290698 | C | A | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.472-425G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290698 | ||||||
chr2:127290713 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472-440A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290713 | ||||||
chr2:127290848 | G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18994.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.472-575C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290848 | ||||||
chr2:127290938 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.472-665G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290938 | ||||||
chr2:127290973 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.472-700A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290973 | ||||||
chr2:127291013 | T | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0005c0011t0001g0235 | 3 | HG01169.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.472-740A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291013 | ||||||
chr2:127291017 | G | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.472-744C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291017 | ||||||
chr2:127291019 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.472-746A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291019 | ||||||
chr2:127291098 | A | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(93): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.472-825T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291098 | ||||||
chr2:127291332 | T | C | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0259 | 3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472-1059A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291332 | ||||||
chr2:127291535 | A | C | 9 | a0001c0001t0001g0031a0001c0001t0001g0130a0001c0001t0001g0131others(6): Show | 10 | HG00408.hp1 HG00438.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+1075T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291535 | ||||||
chr2:127291631 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+979G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291631 | ||||||
chr2:127291720 | G | A | 4 | a0001c0001t0001g0223a0001c0003t0001g0040a0001c0003t0001g0222others(1): Show | 5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+890C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291720 | ||||||
chr2:127291798 | A | G | 1 | a0001c0001t0004g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471+812T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291798 | ||||||
chr2:127292027 | G | A | 2 | a0001c0005t0001g0224a0001c0005t0001g0225 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.471+583C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292027 | ||||||
chr2:127292055 | T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 163 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.471+555A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292055 | ||||||
chr2:127292180 | C | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+430G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292180 | ||||||
chr2:127292200 | T | C | 1 | a0001c0003t0001g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.471+410A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292200 | ||||||
chr2:127292281 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+329G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292281 | ||||||
chr2:127292341 | C | A | 1 | a0001c0001t0001g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.471+269G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292341 | ||||||
chr2:127292369 | GTGGCCTC others(48): Show |
G | 6 | a0001c0001t0001g0228a0001c0001t0002g0043a0001c0001t0002g0262others(3): Show | 7 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+186_471+240del others(55): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292369 | ||||||
chr2:127292424 | A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.471+186T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292424 | ||||||
chr2:127292492 | C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 5 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+118G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292492 | ||||||
chr2:127292558 | T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.471+52A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292558 | ||||||
chr2:127292580 | G | A | 2 | a0001c0004t0001g0042a0001c0004t0001g0234 | 3 | HG01175.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.471+30C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292580 | ||||||
chr2:127292907 | T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.235-61A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 2/14 | chr2 | 127292907 | ||||||
chr2:127293190 | T | C | 1 | a0001c0001t0004g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+323A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 2/14 | chr2 | 127293190 | ||||||
chr2:127293256 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.234+257G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 2/14 | chr2 | 127293256 | ||||||
chr2:127293733 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.29-15G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293733 | ||||||
chr2:127293805 | G | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-87C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293805 | ||||||
chr2:127293843 | G | A | 1 | a0001c0001t0001g0044 | 2 | NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.29-125C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293843 | ||||||
chr2:127293998 | G | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+56C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293998 | ||||||
chr2:127294014 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.28+40T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127294014 |