Item | Value |
---|---|
geneid | 2074 |
ensemblid | ENSG00000225830.16 |
hgncid | 3438 |
symbol | ERCC6 |
name | ERCC excision repair 6, chromatin remodeling factor |
refseq_nuc | NM_000124.4 |
refseq_prot | NP_000115.1 |
ensembl_nuc | ENST00000355832.10 |
ensembl_prot | ENSP00000348089.5 |
mane_status | MANE Select |
chr | chr10 |
start | 49454470 |
end | 49539121 |
strand | - |
ver | v1.2 |
region | chr10:49454470-49539121 |
region5000 | chr10:49449470-49544121 |
regionname0 | ERCC6_chr10_49454470_49539121 |
regionname5000 | ERCC6_chr10_49449470_49544121 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1493 | 173 | 39 | 29 | 78 | 4 | 22 | 60 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002 | 0/1 | 1493 | 81 | 16 | 7 | 54 | 2 | 1 | 40 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0003 | 0/0 | 1493 | 45 | 4 | 15 | 9 | 2 | 15 | 9 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0004 | 0/0 | 1493 | 36 | 2 | 4 | 30 | 0 | 0 | 28 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0005 | 0/0 | 1493 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0006 | 0/0 | 1493 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0007 | 0/0 | 1493 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0008 | 0/0 | 1493 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0009 | 0/0 | 1493 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0010 | 0/0 | 1493 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0011 | 0/0 | 1493 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0012 | 0/0 | 1493 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0013 | 0/0 | 1493 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0014 | 0/0 | 1493 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0015 | 0/0 | 1493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0016 | 0/0 | 1493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0017 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0018 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0019 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0020 | 0/0 | 1493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0021 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0022 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0023 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0024 | 0/0 | 1493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0025 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0026 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0027 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0028 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0029 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0030 | 0/0 | 1493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4482 | 77 | 4 | 16 | 44 | 4 | 9 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0002 | 0/1 | 4482 | 62 | 11 | 2 | 47 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0003 | 0/0 | 4482 | 45 | 4 | 15 | 9 | 2 | 15 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0004 | 1/0 | 4482 | 42 | 30 | 7 | 0 | 0 | 4 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0005 | 0/0 | 4482 | 42 | 3 | 5 | 26 | 0 | 8 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0006 | 0/0 | 4482 | 35 | 2 | 4 | 29 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0007 | 0/0 | 4482 | 15 | 1 | 5 | 7 | 2 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0008 | 0/0 | 4482 | 11 | 9 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0009 | 0/0 | 4482 | 8 | 0 | 1 | 7 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0010 | 0/0 | 4482 | 6 | 4 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0011 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0012 | 0/0 | 4482 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0013 | 0/0 | 4482 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0014 | 0/0 | 4482 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0015 | 0/0 | 4482 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0016 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0017 | 0/0 | 4482 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0018 | 0/0 | 4482 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0019 | 0/0 | 4482 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0020 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0021 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0022 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0023 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0024 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0025 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0026 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0027 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0028 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0029 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0030 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0031 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0032 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0033 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0034 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0035 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0036 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0037 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0038 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0039 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0040 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
c0041 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4520 | 125 | 47 | 25 | 35 | 2 | 15 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0002 | 0/0 | 4520 | 86 | 4 | 20 | 49 | 4 | 9 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0003 | 0/0 | 4520 | 46 | 2 | 5 | 30 | 0 | 9 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0004 | 0/0 | 4520 | 42 | 1 | 5 | 33 | 2 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0005 | 0/0 | 4521 | 14 | 0 | 0 | 14 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0006 | 0/1 | 4520 | 8 | 6 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0007 | 0/0 | 4517 | 7 | 0 | 3 | 0 | 0 | 4 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0008 | 0/0 | 4520 | 6 | 4 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0009 | 0/0 | 4520 | 5 | 2 | 2 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0010 | 0/0 | 4520 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0011 | 0/0 | 4520 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0012 | 0/0 | 4521 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0013 | 0/0 | 4520 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0014 | 0/0 | 4520 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0015 | 0/0 | 4520 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0016 | 0/0 | 4520 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0017 | 0/0 | 4520 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0018 | 0/0 | 4520 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0019 | 0/0 | 4520 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0020 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0021 | 0/0 | 4520 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0022 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0023 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0024 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0025 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0026 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0027 | 0/0 | 4517 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0028 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0029 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0030 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0031 | 0/0 | 4520 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0032 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0033 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0034 | 0/0 | 4520 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0035 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0036 | 0/0 | 4520 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0037 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0038 | 0/0 | 4521 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0039 | 0/0 | 4520 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
t0040 | 0/0 | 4521 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0331 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0341 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4482 | 77 | 4 | 16 | 44 | 4 | 9 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0004 | 1/0 | 4482 | 42 | 30 | 7 | 0 | 0 | 4 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0005 | 0/0 | 4482 | 42 | 3 | 5 | 26 | 0 | 8 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0009 | 0/0 | 4482 | 8 | 0 | 1 | 7 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0029 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0030 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0038 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0001c0040 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0002c0002 | 0/1 | 4482 | 62 | 11 | 2 | 47 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0002c0007 | 0/0 | 4482 | 15 | 1 | 5 | 7 | 2 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0002c0012 | 0/0 | 4482 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0002c0025 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0003c0003 | 0/0 | 4482 | 45 | 4 | 15 | 9 | 2 | 15 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0004c0006 | 0/0 | 4482 | 35 | 2 | 4 | 29 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0004c0023 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0005c0008 | 0/0 | 4482 | 11 | 9 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0006c0010 | 0/0 | 4482 | 6 | 4 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0007c0011 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0008c0014 | 0/0 | 4482 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0009c0013 | 0/0 | 4482 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0010c0017 | 0/0 | 4482 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0011c0015 | 0/0 | 4482 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0012c0018 | 0/0 | 4482 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0013c0019 | 0/0 | 4482 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0014c0016 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0015c0022 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0016c0028 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0017c0020 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0018c0024 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0019c0021 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0020c0031 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0021c0026 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0022c0039 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0023c0027 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0024c0033 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0025c0032 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0026c0041 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0027c0035 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0028c0034 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0029c0036 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 | |
a0030c0037 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 9001 | 70 | 3 | 15 | 40 | 4 | 8 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0001t0019 | 0/0 | 9001 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0001t0023 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0001t0032 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0001t0033 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0001t0034 | 0/0 | 9001 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0001t0036 | 0/0 | 9001 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0004t0001 | 1/0 | 9001 | 30 | 26 | 3 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0004t0007 | 0/0 | 8998 | 7 | 0 | 3 | 0 | 0 | 4 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0004t0011 | 0/0 | 9001 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0004t0027 | 0/0 | 8998 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0005t0003 | 0/0 | 9001 | 40 | 2 | 5 | 25 | 0 | 8 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0005t0025 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0005t0026 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0009t0002 | 0/0 | 9001 | 7 | 0 | 1 | 6 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0009t0035 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0029t0001 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0030t0031 | 0/0 | 9001 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0038t0002 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0001c0040t0002 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0004 | 0/0 | 9001 | 25 | 0 | 0 | 24 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0005 | 0/0 | 9002 | 13 | 0 | 0 | 13 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0006 | 0/1 | 9001 | 8 | 6 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0009 | 0/0 | 9001 | 5 | 2 | 2 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0012 | 0/0 | 9002 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0015 | 0/0 | 9001 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0017 | 0/0 | 9001 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0020 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0037 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0038 | 0/0 | 9002 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0039 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0002t0040 | 0/0 | 9002 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0007t0004 | 0/0 | 9001 | 14 | 1 | 4 | 7 | 2 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0007t0021 | 0/0 | 9001 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0012t0001 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0012t0014 | 0/0 | 9001 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0002c0025t0014 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0003c0003t0001 | 0/0 | 9001 | 45 | 4 | 15 | 9 | 2 | 15 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0004c0006t0001 | 0/0 | 9001 | 31 | 2 | 4 | 25 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0004c0006t0010 | 0/0 | 9001 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0004c0023t0010 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0005c0008t0001 | 0/0 | 9001 | 10 | 8 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0005c0008t0029 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0006c0010t0008 | 0/0 | 9001 | 6 | 4 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0007c0011t0001 | 0/0 | 9001 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0007c0011t0022 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0007c0011t0028 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0008c0014t0003 | 0/0 | 9001 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0009c0013t0013 | 0/0 | 9001 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0010c0017t0003 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0010c0017t0024 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0011c0015t0004 | 0/0 | 9001 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0012c0018t0002 | 0/0 | 9001 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0013c0019t0002 | 0/0 | 9001 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0014c0016t0018 | 0/0 | 9001 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0015c0022t0004 | 0/0 | 9001 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0016c0028t0001 | 0/0 | 9001 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0017c0020t0005 | 0/0 | 9002 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0018c0024t0001 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0019c0021t0012 | 0/0 | 9002 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0020c0031t0002 | 0/0 | 9001 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0021c0026t0030 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0022c0039t0002 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0023c0027t0001 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0024c0033t0003 | 0/0 | 9001 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0025c0032t0016 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0026c0041t0002 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0027c0035t0001 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0028c0034t0001 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0029c0036t0016 | 0/0 | 9001 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
a0030c0037t0003 | 0/0 | 9001 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | copy fasta | chr10 | 49449470 | 49544121 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0019g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0019g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0023g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0032g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0033g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0034g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0001t0036g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0001g0331 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0007g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0007g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0007g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0007g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0011g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0004t0027g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0025g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0005t0026g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0009t0035g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0029t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0030t0031g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0038t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0001c0040t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0341 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0009g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0009g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0012g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0012g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0015g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0015g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0017g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0020g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0037g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0038g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0039g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0002t0040g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0007t0021g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0012t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0012t0014g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0012t0014g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0002c0025t0014g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0010g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0006t0010g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0004c0023t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0005c0008t0029g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0006c0010t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0006c0010t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0006c0010t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0006c0010t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0006c0010t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0006c0010t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0007c0011t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0007c0011t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0007c0011t0022g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0007c0011t0028g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0008c0014t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0008c0014t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0009c0013t0013g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0009c0013t0013g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0010c0017t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0010c0017t0024g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0011c0015t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0011c0015t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0012c0018t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0012c0018t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0013c0019t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0013c0019t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0014c0016t0018g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0015c0022t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0016c0028t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0017c0020t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0018c0024t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0019c0021t0012g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0020c0031t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0021c0026t0030g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0022c0039t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0023c0027t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0024c0033t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0025c0032t0016g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0026c0041t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0027c0035t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0028c0034t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0029c0036t0016g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
a0030c0037t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0007 | t0004 | g0009 | EUR | GBR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | GBR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0097 | EUR | GBR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00280 | hp1 | a0002 | c0007 | t0004 | g0009 | EUR | FIN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00408 | hp2 | a0002 | c0002 | t0004 | g0042 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00438 | hp1 | a0001 | c0005 | t0003 | g0332 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00438 | hp2 | a0002 | c0002 | t0005 | g0084 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00558 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00558 | hp2 | a0001 | c0009 | t0002 | g0017 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00597 | hp1 | a0002 | c0002 | t0005 | g0078 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00597 | hp2 | a0001 | c0005 | t0003 | g0274 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00609 | hp1 | a0001 | c0009 | t0035 | g0193 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00609 | hp2 | a0002 | c0002 | t0004 | g0053 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00621 | hp1 | a0001 | c0005 | t0003 | g0281 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00621 | hp2 | a0002 | c0002 | t0006 | g0340 | EAS | CHS | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00642 | hp1 | a0002 | c0002 | t0009 | g0328 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0103 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00738 | hp2 | a0013 | c0019 | t0002 | g0219 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00741 | hp1 | a0001 | c0005 | t0003 | g0271 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG00741 | hp2 | a0002 | c0002 | t0009 | g0326 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01069 | hp1 | a0005 | c0008 | t0001 | g0014 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01069 | hp2 | a0006 | c0010 | t0008 | g0117 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01070 | hp1 | a0001 | c0004 | t0007 | g0025 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01070 | hp2 | a0004 | c0006 | t0001 | g0307 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01071 | hp1 | a0004 | c0006 | t0001 | g0316 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01071 | hp2 | a0005 | c0008 | t0001 | g0014 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01074 | hp1 | a0001 | c0004 | t0007 | g0025 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01074 | hp2 | a0003 | c0003 | t0001 | g0263 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0109 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01099 | hp1 | a0001 | c0005 | t0003 | g0288 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0283 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01106 | hp1 | a0001 | c0004 | t0007 | g0249 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0107 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0244 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01167 | hp1 | a0001 | c0004 | t0001 | g0146 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0094 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01168 | hp1 | a0004 | c0006 | t0001 | g0302 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01168 | hp2 | a0012 | c0018 | t0002 | g0224 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0095 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01169 | hp2 | a0012 | c0018 | t0002 | g0225 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01192 | hp2 | a0001 | c0004 | t0001 | g0124 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01243 | hp2 | a0009 | c0013 | t0013 | g0034 | AMR | PUR | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0261 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01258 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0105 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01261 | hp2 | a0015 | c0022 | t0004 | g0062 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0262 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01346 | hp2 | a0001 | c0005 | t0003 | g0289 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0102 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0112 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01496 | hp1 | a0002 | c0007 | t0004 | g0069 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0137 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0251 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01891 | hp1 | a0002 | c0002 | t0006 | g0334 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01891 | hp2 | a0002 | c0012 | t0001 | g0113 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01928 | hp1 | a0002 | c0007 | t0021 | g0067 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01928 | hp2 | a0001 | c0009 | t0002 | g0167 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01934 | hp1 | a0004 | c0006 | t0001 | g0310 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01934 | hp2 | a0003 | c0003 | t0001 | g0111 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01952 | hp2 | a0001 | c0005 | t0003 | g0297 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01978 | hp2 | a0001 | c0005 | t0003 | g0299 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01981 | hp1 | a0016 | c0028 | t0001 | g0091 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01981 | hp2 | a0002 | c0007 | t0004 | g0072 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02015 | hp2 | a0002 | c0007 | t0004 | g0061 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02027 | hp1 | a0001 | c0005 | t0003 | g0275 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0246 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02056 | hp2 | a0004 | c0006 | t0010 | g0317 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02071 | hp1 | a0002 | c0002 | t0005 | g0046 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02071 | hp2 | a0001 | c0005 | t0003 | g0273 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02074 | hp1 | a0002 | c0002 | t0020 | g0081 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02074 | hp2 | a0002 | c0002 | t0038 | g0339 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02083 | hp1 | a0002 | c0007 | t0004 | g0073 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02132 | hp2 | a0002 | c0002 | t0005 | g0083 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02145 | hp1 | a0009 | c0013 | t0013 | g0329 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02145 | hp2 | a0007 | c0011 | t0001 | g0253 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CDX | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02155 | hp2 | a0010 | c0017 | t0003 | g0258 | EAS | CDX | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02165 | hp1 | a0002 | c0002 | t0004 | g0054 | EAS | CDX | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02257 | hp2 | a0003 | c0003 | t0001 | g0136 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02258 | hp1 | a0005 | c0008 | t0001 | g0132 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02273 | hp2 | a0002 | c0007 | t0004 | g0066 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02293 | hp1 | a0013 | c0019 | t0002 | g0214 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02293 | hp2 | a0001 | c0004 | t0027 | g0250 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02300 | hp1 | a0002 | c0007 | t0004 | g0077 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02300 | hp2 | a0001 | c0001 | t0036 | g0233 | AMR | PEL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02451 | hp1 | a0002 | c0002 | t0039 | g0335 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02451 | hp2 | a0001 | c0029 | t0001 | g0152 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02523 | hp1 | a0001 | c0005 | t0003 | g0295 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02523 | hp2 | a0002 | c0002 | t0015 | g0056 | EAS | KHV | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02572 | hp1 | a0001 | c0040 | t0002 | g0245 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02572 | hp2 | a0005 | c0008 | t0001 | g0130 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02615 | hp1 | a0004 | c0006 | t0001 | g0311 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02615 | hp2 | a0006 | c0010 | t0008 | g0119 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0125 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02630 | hp1 | a0002 | c0012 | t0014 | g0323 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02647 | hp1 | a0001 | c0005 | t0025 | g0156 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0150 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02683 | hp1 | a0001 | c0001 | t0034 | g0176 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02683 | hp2 | a0003 | c0003 | t0001 | g0101 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02698 | hp1 | a0003 | c0003 | t0001 | g0104 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02698 | hp2 | a0001 | c0005 | t0003 | g0027 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02717 | hp1 | a0002 | c0002 | t0006 | g0333 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02717 | hp2 | a0007 | c0011 | t0022 | g0090 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02723 | hp1 | a0002 | c0002 | t0017 | g0327 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0247 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0100 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02809 | hp1 | a0002 | c0002 | t0006 | g0343 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02809 | hp2 | a0021 | c0026 | t0030 | g0330 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02818 | hp1 | a0001 | c0004 | t0001 | g0151 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02818 | hp2 | a0023 | c0027 | t0001 | g0248 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02886 | hp1 | a0014 | c0016 | t0018 | g0035 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02886 | hp2 | a0006 | c0010 | t0008 | g0154 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02895 | hp1 | a0002 | c0012 | t0014 | g0325 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02896 | hp2 | a0001 | c0004 | t0011 | g0024 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02922 | hp1 | a0002 | c0002 | t0009 | g0012 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02922 | hp2 | a0006 | c0010 | t0008 | g0118 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0242 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0144 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02976 | hp1 | a0005 | c0008 | t0001 | g0128 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02976 | hp2 | a0002 | c0025 | t0014 | g0324 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03017 | hp1 | a0001 | c0004 | t0007 | g0240 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0106 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03041 | hp1 | a0029 | c0036 | t0016 | g0093 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03041 | hp2 | a0001 | c0005 | t0003 | g0278 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03098 | hp2 | a0006 | c0010 | t0008 | g0115 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03130 | hp1 | a0002 | c0002 | t0006 | g0336 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0122 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03139 | hp1 | a0001 | c0004 | t0001 | g0235 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0300 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03195 | hp2 | a0014 | c0016 | t0018 | g0035 | AFR | ESN | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03209 | hp1 | a0005 | c0008 | t0029 | g0139 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03209 | hp2 | a0001 | c0004 | t0011 | g0116 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03225 | hp1 | a0004 | c0006 | t0001 | g0318 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03225 | hp2 | a0028 | c0034 | t0001 | g0121 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03239 | hp1 | a0001 | c0004 | t0007 | g0238 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0153 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0123 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03486 | hp1 | a0018 | c0024 | t0001 | g0322 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03486 | hp2 | a0002 | c0002 | t0017 | g0120 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03491 | hp1 | a0001 | c0004 | t0007 | g0241 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03491 | hp2 | a0001 | c0005 | t0003 | g0280 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03492 | hp1 | a0001 | c0004 | t0007 | g0239 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03540 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0098 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03669 | hp1 | a0002 | c0002 | t0004 | g0051 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0099 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0010 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03710 | hp1 | a0001 | c0005 | t0003 | g0256 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0110 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03831 | hp2 | a0001 | c0005 | t0003 | g0027 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0127 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03834 | hp2 | a0001 | c0005 | t0003 | g0285 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03927 | hp2 | a0001 | c0005 | t0003 | g0268 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0135 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04115 | hp1 | a0001 | c0005 | t0003 | g0279 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04184 | hp1 | a0001 | c0005 | t0003 | g0276 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04184 | hp2 | a0020 | c0031 | t0002 | g0215 | SAS | BEB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04199 | hp1 | a0024 | c0033 | t0003 | g0296 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0126 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04228 | hp1 | a0001 | c0030 | t0031 | g0175 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG04228 | hp2 | a0003 | c0003 | t0001 | g0138 | SAS | STU | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18522 | hp1 | a0005 | c0008 | t0001 | g0129 | AFR | YRI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18522 | hp2 | a0007 | c0011 | t0001 | g0255 | AFR | YRI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18612 | hp2 | a0004 | c0006 | t0001 | g0305 | EAS | CHB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18747 | hp1 | a0010 | c0017 | t0024 | g0259 | EAS | CHB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18906 | hp1 | a0002 | c0002 | t0006 | g0338 | AFR | YRI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18906 | hp2 | a0009 | c0013 | t0013 | g0034 | AFR | YRI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18939 | hp1 | a0002 | c0002 | t0004 | g0041 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18940 | hp1 | a0001 | c0001 | t0019 | g0217 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18940 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18941 | hp1 | a0004 | c0006 | t0001 | g0308 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18942 | hp1 | a0001 | c0005 | t0003 | g0029 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0043 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18943 | hp1 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18944 | hp1 | a0001 | c0005 | t0003 | g0003 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18944 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18945 | hp1 | a0001 | c0005 | t0003 | g0257 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18945 | hp2 | a0002 | c0007 | t0004 | g0065 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18946 | hp1 | a0002 | c0002 | t0004 | g0057 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18947 | hp2 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18948 | hp1 | a0011 | c0015 | t0004 | g0037 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18948 | hp2 | a0004 | c0006 | t0001 | g0031 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18949 | hp2 | a0004 | c0006 | t0001 | g0315 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18950 | hp1 | a0002 | c0002 | t0005 | g0085 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18950 | hp2 | a0004 | c0006 | t0001 | g0301 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18951 | hp2 | a0004 | c0006 | t0001 | g0033 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18953 | hp1 | a0002 | c0002 | t0037 | g0342 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18953 | hp2 | a0008 | c0014 | t0003 | g0282 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18954 | hp1 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18954 | hp2 | a0004 | c0006 | t0001 | g0312 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18957 | hp1 | a0002 | c0002 | t0040 | g0344 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18957 | hp2 | a0001 | c0005 | t0026 | g0092 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18959 | hp2 | a0027 | c0035 | t0001 | g0265 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18961 | hp1 | a0004 | c0006 | t0001 | g0023 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18961 | hp2 | a0001 | c0001 | t0033 | g0172 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18962 | hp1 | a0002 | c0007 | t0004 | g0071 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18962 | hp2 | a0004 | c0006 | t0001 | g0321 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18963 | hp1 | a0002 | c0002 | t0005 | g0045 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18963 | hp2 | a0001 | c0009 | t0002 | g0159 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18966 | hp1 | a0004 | c0006 | t0001 | g0319 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18966 | hp2 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18968 | hp2 | a0008 | c0014 | t0003 | g0028 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18970 | hp1 | a0004 | c0006 | t0001 | g0306 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18970 | hp2 | a0002 | c0002 | t0004 | g0087 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18971 | hp1 | a0001 | c0038 | t0002 | g0184 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18971 | hp2 | a0030 | c0037 | t0003 | g0287 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18972 | hp2 | a0002 | c0002 | t0012 | g0161 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18973 | hp1 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18973 | hp2 | a0001 | c0005 | t0003 | g0291 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18974 | hp2 | a0001 | c0005 | t0003 | g0269 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18975 | hp2 | a0019 | c0021 | t0012 | g0205 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18977 | hp1 | a0004 | c0006 | t0001 | g0022 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18977 | hp2 | a0017 | c0020 | t0005 | g0060 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18978 | hp1 | a0002 | c0002 | t0004 | g0059 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18979 | hp1 | a0002 | c0002 | t0005 | g0047 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18979 | hp2 | a0001 | c0009 | t0002 | g0164 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18982 | hp1 | a0001 | c0005 | t0003 | g0003 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18982 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18983 | hp1 | a0001 | c0005 | t0003 | g0003 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18984 | hp1 | a0001 | c0009 | t0002 | g0189 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18984 | hp2 | a0004 | c0006 | t0010 | g0006 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18985 | hp2 | a0001 | c0005 | t0003 | g0267 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18986 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18989 | hp1 | a0001 | c0005 | t0003 | g0286 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18989 | hp2 | a0002 | c0002 | t0009 | g0204 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18990 | hp2 | a0002 | c0002 | t0004 | g0086 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18993 | hp1 | a0004 | c0006 | t0001 | g0032 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18994 | hp1 | a0004 | c0006 | t0001 | g0313 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18995 | hp1 | a0002 | c0002 | t0004 | g0075 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18999 | hp2 | a0004 | c0006 | t0001 | g0303 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19000 | hp1 | a0001 | c0005 | t0003 | g0294 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19000 | hp2 | a0002 | c0007 | t0004 | g0064 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19002 | hp1 | a0002 | c0002 | t0004 | g0089 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19004 | hp2 | a0004 | c0006 | t0001 | g0314 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19005 | hp1 | a0002 | c0007 | t0004 | g0070 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19005 | hp2 | a0001 | c0005 | t0003 | g0272 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19006 | hp1 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19006 | hp2 | a0002 | c0007 | t0004 | g0063 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19007 | hp1 | a0004 | c0006 | t0010 | g0006 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19007 | hp2 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19009 | hp1 | a0002 | c0002 | t0004 | g0039 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19010 | hp2 | a0002 | c0002 | t0012 | g0162 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19011 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19011 | hp2 | a0001 | c0009 | t0002 | g0320 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19012 | hp1 | a0002 | c0002 | t0005 | g0088 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19012 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19043 | hp1 | a0005 | c0008 | t0001 | g0133 | AFR | LWK | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19043 | hp2 | a0002 | c0002 | t0006 | g0337 | AFR | LWK | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19054 | hp1 | a0004 | c0006 | t0001 | g0022 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19054 | hp2 | a0002 | c0002 | t0004 | g0074 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19056 | hp1 | a0002 | c0002 | t0015 | g0055 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19056 | hp2 | a0004 | c0006 | t0001 | g0031 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19057 | hp1 | a0008 | c0014 | t0003 | g0028 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19060 | hp2 | a0002 | c0002 | t0004 | g0040 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19063 | hp1 | a0011 | c0015 | t0004 | g0038 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19063 | hp2 | a0004 | c0023 | t0010 | g0309 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19064 | hp1 | a0001 | c0001 | t0019 | g0220 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19064 | hp2 | a0001 | c0005 | t0003 | g0029 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19066 | hp1 | a0004 | c0006 | t0001 | g0304 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19067 | hp2 | a0002 | c0002 | t0005 | g0076 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19068 | hp1 | a0001 | c0005 | t0003 | g0270 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19068 | hp2 | a0004 | c0006 | t0001 | g0023 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19070 | hp1 | a0002 | c0002 | t0004 | g0058 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19070 | hp2 | a0001 | c0005 | t0003 | g0260 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19072 | hp2 | a0001 | c0005 | t0003 | g0284 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19074 | hp1 | a0001 | c0005 | t0003 | g0003 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19074 | hp2 | a0004 | c0006 | t0001 | g0032 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19075 | hp2 | a0001 | c0005 | t0003 | g0293 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19076 | hp1 | a0022 | c0039 | t0002 | g0185 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19076 | hp2 | a0002 | c0002 | t0005 | g0050 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19077 | hp1 | a0004 | c0006 | t0001 | g0236 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19077 | hp2 | a0002 | c0002 | t0005 | g0052 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19084 | hp1 | a0004 | c0006 | t0010 | g0006 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19085 | hp1 | a0001 | c0009 | t0002 | g0017 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19085 | hp2 | a0001 | c0005 | t0003 | g0292 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19087 | hp2 | a0001 | c0001 | t0023 | g0206 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19088 | hp1 | a0004 | c0006 | t0001 | g0033 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19088 | hp2 | a0002 | c0002 | t0005 | g0080 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19089 | hp1 | a0026 | c0041 | t0002 | g0174 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19089 | hp2 | a0002 | c0002 | t0005 | g0036 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19090 | hp2 | a0002 | c0002 | t0004 | g0082 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19240 | hp1 | a0002 | c0002 | t0009 | g0012 | AFR | YRI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0140 | AFR | YRI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA20129 | hp1 | a0001 | c0004 | t0011 | g0237 | AFR | ASW | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA20129 | hp2 | a0001 | c0005 | t0003 | g0298 | AFR | ASW | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA20752 | hp1 | a0003 | c0003 | t0001 | g0108 | EUR | TSI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | TSI | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01123 | hp1 | a0006 | c0010 | t0008 | g0114 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02109 | hp1 | a0005 | c0008 | t0001 | g0131 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02109 | hp2 | a0001 | c0001 | t0032 | g0228 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02486 | hp1 | a0005 | c0008 | t0001 | g0141 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0243 | AFR | ACB | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03471 | hp1 | a0025 | c0032 | t0016 | g0155 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0148 | AFR | MSL | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG06807 | hp1 | a0005 | c0008 | t0001 | g0134 | AFR | USA | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | USA | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA18955 | hp2 | a0001 | c0005 | t0003 | g0290 | EAS | JPT | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA20300 | hp1 | a0001 | c0004 | t0011 | g0024 | AFR | USA | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA20300 | hp2 | a0002 | c0007 | t0004 | g0068 | AFR | USA | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0254 | AFR | LWK | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
NA21309 | hp2 | a0007 | c0011 | t0028 | g0252 | AFR | LWK | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0006 | g0341 | REF | REF | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0331 | REF | REF | ERCC6_chr10_49449470_49544121 | ERCC6 | chr10 | 49449470 | 49544121 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49458867 | T | C | 1 | a0017 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.4430A>G | p.His1477Arg | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4604/9001 | 4430/4482 | 1477/1493 | chr10 | 49458867 | ||
chr10:49458975 | G | A | 1 | a0005 | 11 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(8): Show |
missense_variant | MODERATE | c.4322C>T | p.Thr1441Ile | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4496/9001 | 4322/4482 | 1441/1493 | chr10 | 49458975 | ||
chr10:49459059 | T | C | 3 | a0003a0005a0027 | 57 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(54): Show |
missense_variant | MODERATE | c.4238A>G | p.Gln1413Arg | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4412/9001 | 4238/4482 | 1413/1493 | chr10 | 49459059 | ||
chr10:49459183 | C | T | 2 | a0016a0018 | 2 | HG01981.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.4114G>A | p.Gly1372Arg | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4288/9001 | 4114/4482 | 1372/1493 | chr10 | 49459183 | ||
chr10:49459202 | A | T | 1 | a0029 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.4095T>A | p.Asn1365Lys | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4269/9001 | 4095/4482 | 1365/1493 | chr10 | 49459202 | ||
chr10:49459232 | A | C | 1 | a0023 | 1 | HG02818.hp2 | missense_variant&splice_region_variant | MODERATE | c.4065T>G | p.Asp1355Glu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4239/9001 | 4065/4482 | 1355/1493 | chr10 | 49459232 | ||
chr10:49461370 | C | A | 1 | a0024 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.3965G>T | p.Gly1322Val | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/21 | 4139/9001 | 3965/4482 | 1322/1493 | chr10 | 49461370 | ||
chr10:49461413 | C | G | 2 | a0009a0014 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.3922G>C | p.Val1308Leu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/21 | 4096/9001 | 3922/4482 | 1308/1493 | chr10 | 49461413 | ||
chr10:49461443 | T | C | 1 | a0022 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.3892A>G | p.Arg1298Gly | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/21 | 4066/9001 | 3892/4482 | 1298/1493 | chr10 | 49461443 | ||
chr10:49461517 | T | C | 1 | a0019 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.3818A>G | p.Asp1273Gly | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/21 | 3992/9001 | 3818/4482 | 1273/1493 | chr10 | 49461517 | ||
chr10:49470215 | C | T | 1 | a0025 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.3745G>A | p.Asp1249Asn | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3919/9001 | 3745/4482 | 1249/1493 | chr10 | 49470215 | ||
chr10:49470241 | C | A | 1 | a0016 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.3719G>T | p.Ser1240Ile | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3893/9001 | 3719/4482 | 1240/1493 | chr10 | 49470241 | ||
chr10:49470271 | C | G | 1 | a0004 | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
missense_variant | MODERATE | c.3689G>C | p.Arg1230Pro | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3863/9001 | 3689/4482 | 1230/1493 | chr10 | 49470271 | ||
chr10:49470301 | G | A | 2 | a0014a0021 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.3659C>T | p.Thr1220Ile | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3833/9001 | 3659/4482 | 1220/1493 | chr10 | 49470301 | ||
chr10:49470323 | T | C | 4 | a0003a0005a0007others(1): Show | 61 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(58): Show |
missense_variant | MODERATE | c.3637A>G | p.Arg1213Gly | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3811/9001 | 3637/4482 | 1213/1493 | chr10 | 49470323 | ||
chr10:49470379 | T | C | 1 | a0026 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.3581A>G | p.Glu1194Gly | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3755/9001 | 3581/4482 | 1194/1493 | chr10 | 49470379 | ||
chr10:49470478 | C | G | 1 | a0028 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.3482G>C | p.Ser1161Thr | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3656/9001 | 3482/4482 | 1161/1493 | chr10 | 49470478 | ||
chr10:49470479 | T | G | 1 | a0028 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.3481A>C | p.Ser1161Arg | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3655/9001 | 3481/4482 | 1161/1493 | chr10 | 49470479 | ||
chr10:49470524 | T | C | 1 | a0027 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.3436A>G | p.Ser1146Gly | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3610/9001 | 3436/4482 | 1146/1493 | chr10 | 49470524 | ||
chr10:49470671 | T | C | 4 | a0003a0005a0027others(1): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
missense_variant | MODERATE | c.3289A>G | p.Met1097Val | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3463/9001 | 3289/4482 | 1097/1493 | chr10 | 49470671 | ||
chr10:49470676 | G | C | 1 | a0029 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.3284C>G | p.Pro1095Arg | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3458/9001 | 3284/4482 | 1095/1493 | chr10 | 49470676 | ||
chr10:49470769 | T | C | 1 | a0030 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.3191A>G | p.Asn1064Ser | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3365/9001 | 3191/4482 | 1064/1493 | chr10 | 49470769 | ||
chr10:49472425 | C | A | 1 | a0013 | 2 | HG00738.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.2875G>T | p.Val959Leu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/21 | 3049/9001 | 2875/4482 | 959/1493 | chr10 | 49472425 | ||
chr10:49472913 | G | A | 1 | a0006 | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
missense_variant | MODERATE | c.2825C>T | p.Thr942Met | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 15/21 | 2999/9001 | 2825/4482 | 942/1493 | chr10 | 49472913 | ||
chr10:49473024 | G | A | 1 | a0011 | 2 | NA18948.hp1 NA19063.hp1 |
missense_variant | MODERATE | c.2714C>T | p.Thr905Ile | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 15/21 | 2888/9001 | 2714/4482 | 905/1493 | chr10 | 49473024 | ||
chr10:49473485 | A | G | 1 | a0020 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.2701T>C | p.Tyr901His | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 14/21 | 2875/9001 | 2701/4482 | 901/1493 | chr10 | 49473485 | ||
chr10:49474115 | C | T | 1 | a0008 | 3 | NA18953.hp2 NA18968.hp2 NA19057.hp1 |
missense_variant | MODERATE | c.2510G>A | p.Arg837His | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 13/21 | 2684/9001 | 2510/4482 | 837/1493 | chr10 | 49474115 | ||
chr10:49474230 | G | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.2395C>T | p.Leu799Phe | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 13/21 | 2569/9001 | 2395/4482 | 799/1493 | chr10 | 49474230 | ||
chr10:49524093 | C | T | 1 | a0012 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1337G>A | p.Gly446Asp | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/21 | 1511/9001 | 1337/4482 | 446/1493 | chr10 | 49524093 | ||
chr10:49524234 | C | T | 8 | a0002a0004a0011others(5): Show | 124 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(121): Show |
missense_variant | MODERATE | c.1196G>A | p.Gly399Asp | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/21 | 1370/9001 | 1196/4482 | 399/1493 | chr10 | 49524234 | ||
chr10:49532580 | C | T | 1 | a0010 | 2 | HG02155.hp2 NA18747.hp1 |
missense_variant | MODERATE | c.385G>A | p.Val129Met | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/21 | 559/9001 | 385/4482 | 129/1493 | chr10 | 49532580 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49458911 | C | T | 1 | a0004c0023 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.4386G>A | p.Gln1462Gln | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4560/9001 | 4386/4482 | 1462/1493 | chr10 | 49458911 | ||
chr10:49459139 | G | A | 1 | a0001c0040 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.4158C>T | p.Ser1386Ser | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4332/9001 | 4158/4482 | 1386/1493 | chr10 | 49459139 | ||
chr10:49470186 | T | C | 2 | a0014c0016a0021c0026 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.3774A>G | p.Lys1258Lys | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3948/9001 | 3774/4482 | 1258/1493 | chr10 | 49470186 | ||
chr10:49470774 | A | G | 2 | a0001c0038a0022c0039 | 2 | NA18971.hp1 NA19076.hp1 |
synonymous_variant | LOW | c.3186T>C | p.Ser1062Ser | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3360/9001 | 3186/4482 | 1062/1493 | chr10 | 49470774 | ||
chr10:49470837 | T | C | 1 | a0001c0040 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3123A>G | p.Gln1041Gln | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/21 | 3297/9001 | 3123/4482 | 1041/1493 | chr10 | 49470837 | ||
chr10:49471035 | G | A | 2 | a0001c0009a0026c0041 | 9 | HG00558.hp2 HG00609.hp1 HG01928.hp2 others(6): Show |
synonymous_variant | LOW | c.3010C>T | p.Leu1004Leu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 17/21 | 3184/9001 | 3010/4482 | 1004/1493 | chr10 | 49471035 | ||
chr10:49472987 | G | A | 10 | a0001c0001a0001c0009a0001c0030others(7): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
synonymous_variant | LOW | c.2751C>T | p.Gly917Gly | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 15/21 | 2925/9001 | 2751/4482 | 917/1493 | chr10 | 49472987 | ||
chr10:49474222 | G | A | 1 | a0002c0025 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2403C>T | p.Ala801Ala | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 13/21 | 2577/9001 | 2403/4482 | 801/1493 | chr10 | 49474222 | ||
chr10:49482774 | C | T | 2 | a0014c0016a0021c0026 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.2082G>A | p.Pro694Pro | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/21 | 2256/9001 | 2082/4482 | 694/1493 | chr10 | 49482774 | ||
chr10:49482834 | A | T | 1 | a0001c0030 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.2022T>A | p.Ser674Ser | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/21 | 2196/9001 | 2022/4482 | 674/1493 | chr10 | 49482834 | ||
chr10:49524284 | C | T | 1 | a0007c0011 | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.1146G>A | p.Glu382Glu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/21 | 1320/9001 | 1146/4482 | 382/1493 | chr10 | 49524284 | ||
chr10:49530735 | T | C | 2 | a0002c0007a0015c0022 | 16 | HG00099.hp1 HG00280.hp1 HG01261.hp2 others(13): Show |
synonymous_variant | LOW | c.528A>G | p.Arg176Arg | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/21 | 702/9001 | 528/4482 | 176/1493 | chr10 | 49530735 | ||
chr10:49530825 | G | A | 1 | a0016c0028 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.438C>T | p.Ser146Ser | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/21 | 612/9001 | 438/4482 | 146/1493 | chr10 | 49530825 | ||
chr10:49532554 | C | T | 6 | a0002c0002a0002c0007a0011c0015others(3): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
synonymous_variant | LOW | c.411G>A | p.Leu137Leu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/21 | 585/9001 | 411/4482 | 137/1493 | chr10 | 49532554 | ||
chr10:49532809 | G | A | 1 | a0001c0029 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.156C>T | p.Asp52Asp | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/21 | 330/9001 | 156/4482 | 52/1493 | chr10 | 49532809 | ||
chr10:49532830 | G | C | 21 | a0001c0001a0001c0005a0001c0009others(18): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
synonymous_variant | LOW | c.135C>G | p.Leu45Leu | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/21 | 309/9001 | 135/4482 | 45/1493 | chr10 | 49532830 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49454490 | C | T | 1 | a0006c0010t0008 | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4325G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4325 | chr10 | 49454490 | |||||
chr10:49454506 | A | G | 1 | a0002c0002t0037 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4309T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4309 | chr10 | 49454506 | |||||
chr10:49454678 | T | C | 1 | a0007c0011t0022 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4137A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4137 | chr10 | 49454678 | |||||
chr10:49454725 | C | T | 1 | a0001c0001t0033 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4090G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 4090 | chr10 | 49454725 | |||||
chr10:49454861 | G | A | 1 | a0001c0001t0034 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3954C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3954 | chr10 | 49454861 | |||||
chr10:49454894 | T | C | 1 | a0002c0002t0017 | 2 | HG02723.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3921A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3921 | chr10 | 49454894 | |||||
chr10:49454992 | A | G | 18 | a0002c0002t0004a0002c0002t0005a0002c0002t0006others(15): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3823T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3823 | chr10 | 49454992 | |||||
chr10:49455039 | C | CA | 6 | a0002c0002t0005a0002c0002t0012a0002c0002t0038others(3): Show | 19 | HG00438.hp2 HG00597.hp1 HG02071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3775dupT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3775 | chr10 | 49455039 | |||||
chr10:49455284 | C | T | 1 | a0001c0001t0032 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3531G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3531 | chr10 | 49455284 | |||||
chr10:49455343 | T | A | 1 | a0002c0002t0039 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3472A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3472 | chr10 | 49455343 | |||||
chr10:49455420 | T | G | 2 | a0009c0013t0013a0014c0016t0018 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3395A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3395 | chr10 | 49455420 | |||||
chr10:49455742 | C | T | 1 | a0010c0017t0024 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3073G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 3073 | chr10 | 49455742 | |||||
chr10:49455868 | C | T | 1 | a0001c0001t0019 | 2 | NA18940.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2947G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2947 | chr10 | 49455868 | |||||
chr10:49455869 | G | A | 2 | a0004c0006t0010a0004c0023t0010 | 5 | HG02056.hp2 NA18984.hp2 NA19007.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2946C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2946 | chr10 | 49455869 | |||||
chr10:49455965 | T | C | 1 | a0001c0009t0035 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2850A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2850 | chr10 | 49455965 | |||||
chr10:49456032 | T | C | 1 | a0002c0007t0021 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2783A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2783 | chr10 | 49456032 | |||||
chr10:49456135 | T | G | 1 | a0001c0001t0036 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2680A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2680 | chr10 | 49456135 | |||||
chr10:49456148 | A | G | 1 | a0002c0002t0020 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2667 | chr10 | 49456148 | |||||
chr10:49456578 | G | A | 1 | a0002c0002t0015 | 2 | HG02523.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2237C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2237 | chr10 | 49456578 | |||||
chr10:49456660 | A | G | 1 | a0009c0013t0013 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2155T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2155 | chr10 | 49456660 | |||||
chr10:49456678 | T | C | 4 | a0002c0012t0014a0002c0025t0014a0014c0016t0018others(1): Show | 6 | HG02630.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2137A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2137 | chr10 | 49456678 | |||||
chr10:49456694 | A | T | 1 | a0005c0008t0029 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2121T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2121 | chr10 | 49456694 | |||||
chr10:49456696 | G | A | 2 | a0014c0016t0018a0021c0026t0030 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2119C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 2119 | chr10 | 49456696 | |||||
chr10:49456848 | CAAT | C | 2 | a0001c0004t0007a0001c0004t0027 | 8 | HG01070.hp1 HG01074.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1964_*1966delATT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 1964 | chr10 | 49456848 | |||||
chr10:49456943 | G | A | 2 | a0001c0004t0011a0001c0005t0025 | 5 | HG02647.hp1 HG02896.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1872C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 1872 | chr10 | 49456943 | |||||
chr10:49456985 | A | G | 18 | a0002c0002t0004a0002c0002t0005a0002c0002t0006others(15): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1830T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 1830 | chr10 | 49456985 | |||||
chr10:49457035 | A | G | 1 | a0007c0011t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 1780 | chr10 | 49457035 | |||||
chr10:49457375 | A | G | 1 | a0001c0004t0027 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1440T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 1440 | chr10 | 49457375 | |||||
chr10:49457540 | G | C | 2 | a0002c0012t0014a0002c0025t0014 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 1275 | chr10 | 49457540 | |||||
chr10:49457882 | C | T | 7 | a0001c0005t0003a0001c0005t0026a0008c0014t0003others(4): Show | 48 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*933G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 933 | chr10 | 49457882 | |||||
chr10:49458051 | T | C | 1 | a0001c0005t0026 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 764 | chr10 | 49458051 | |||||
chr10:49458134 | C | T | 1 | a0001c0030t0031 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*681G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 681 | chr10 | 49458134 | |||||
chr10:49458436 | G | C | 17 | a0001c0001t0002a0001c0001t0019a0001c0001t0023others(14): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*379C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 379 | chr10 | 49458436 | |||||
chr10:49458762 | A | G | 10 | a0001c0005t0003a0001c0005t0025a0001c0005t0026others(7): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*53T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 53 | chr10 | 49458762 | |||||
chr10:49458807 | A | T | 1 | a0001c0001t0023 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 21/21 | 8 | chr10 | 49458807 | |||||
chr10:49538969 | C | T | 1 | a0007c0011t0022 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/21 | 6005 | chr10 | 49538969 | |||||
chr10:49539025 | C | A | 4 | a0002c0002t0006a0002c0002t0037a0002c0002t0038others(1): Show | 11 | HG00621.hp2 HG01891.hp1 HG02074.hp2 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/21 | chr10 | 49539025 | ||||||
chr10:49539034 | G | T | 10 | a0002c0002t0004a0002c0002t0005a0002c0002t0015others(7): Show | 61 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-87C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/21 | 6070 | chr10 | 49539034 | |||||
chr10:49539054 | T | G | 1 | a0002c0002t0040 | 1 | NA18957.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/21 | 6090 | chr10 | 49539054 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:49459399 | T | C | 107 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(104): Show | 119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.4063-165A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 20/20 | chr10 | 49459399 | ||||||
chr10:49459508 | G | A | 5 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(2): Show | 5 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.4063-274C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 20/20 | chr10 | 49459508 | ||||||
chr10:49460200 | G | T | 1 | a0002c0002t0039g0335 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4062+173C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 20/20 | chr10 | 49460200 | ||||||
chr10:49460227 | A | G | 2 | a0002c0002t0017g0120a0002c0002t0017g0327 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4062+146T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 20/20 | chr10 | 49460227 | ||||||
chr10:49460359 | G | A | 1 | a0004c0006t0010g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4062+14C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 20/20 | chr10 | 49460359 | ||||||
chr10:49460646 | C | T | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.3984-195G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49460646 | ||||||
chr10:49460750 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3984-299C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49460750 | ||||||
chr10:49460863 | C | T | 1 | a0002c0002t0015g0055 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3984-412G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49460863 | ||||||
chr10:49460984 | G | C | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3983+368C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49460984 | ||||||
chr10:49461116 | A | G | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.3983+236T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49461116 | ||||||
chr10:49461123 | C | T | 76 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(73): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3983+229G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49461123 | ||||||
chr10:49461178 | G | A | 3 | a0009c0013t0013g0034a0009c0013t0013g0329a0014c0016t0018g0035 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3983+174C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49461178 | ||||||
chr10:49461263 | A | G | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3983+89T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 19/20 | chr10 | 49461263 | ||||||
chr10:49461687 | T | C | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.3779-131A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461687 | ||||||
chr10:49461748 | A | C | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.3779-192T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461748 | ||||||
chr10:49461766 | T | C | 1 | a0001c0004t0027g0250 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3779-210A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461766 | ||||||
chr10:49461774 | C | T | 137 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(134): Show | 153 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.3779-218G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461774 | ||||||
chr10:49461840 | T | C | 126 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(123): Show | 144 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3779-284A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461840 | ||||||
chr10:49461846 | T | A | 2 | a0003c0003t0001g0097a0003c0003t0001g0099 | 2 | HG00140.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3779-290A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461846 | ||||||
chr10:49461905 | T | C | 1 | a0001c0005t0003g0273 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3779-349A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461905 | ||||||
chr10:49461923 | C | T | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.3779-367G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49461923 | ||||||
chr10:49462123 | T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0226 | 4 | HG01952.hp1 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.3779-567A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462123 | ||||||
chr10:49462211 | A | C | 128 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(125): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.3779-655T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462211 | ||||||
chr10:49462217 | C | T | 2 | a0001c0004t0001g0140a0001c0004t0001g0145 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3779-661G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462217 | ||||||
chr10:49462297 | C | T | 3 | a0009c0013t0013g0034a0009c0013t0013g0329a0014c0016t0018g0035 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3779-741G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462297 | ||||||
chr10:49462312 | G | A | 6 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(3): Show | 6 | HG01981.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3779-756C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462312 | ||||||
chr10:49462419 | A | G | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3779-863T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462419 | ||||||
chr10:49462424 | G | A | 1 | a0002c0025t0014g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3779-868C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462424 | ||||||
chr10:49462498 | T | A | 2 | a0004c0006t0001g0307a0004c0006t0001g0316 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3779-942A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462498 | ||||||
chr10:49462498 | T | TA | 40 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(37): Show | 49 | HG01168.hp1 HG01192.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.3779-943dupT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462498 | ||||||
chr10:49462544 | C | T | 128 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(125): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.3779-988G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462544 | ||||||
chr10:49462773 | A | G | 1 | a0002c0025t0014g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3779-1217T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462773 | ||||||
chr10:49462837 | T | C | 1 | a0002c0002t0009g0012 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3779-1281A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49462837 | ||||||
chr10:49463009 | C | G | 1 | a0001c0004t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3779-1453G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463009 | ||||||
chr10:49463165 | C | G | 76 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(73): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3779-1609G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463165 | ||||||
chr10:49463399 | T | C | 11 | a0001c0001t0002g0021a0001c0001t0002g0158a0001c0001t0002g0213others(8): Show | 12 | HG00738.hp2 HG02015.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.3779-1843A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463399 | ||||||
chr10:49463700 | C | A | 339 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(336): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.3779-2144G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463700 | ||||||
chr10:49463775 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3779-2219G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463775 | ||||||
chr10:49463865 | C | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3779-2309G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463865 | ||||||
chr10:49463870 | C | T | 2 | a0001c0004t0007g0249a0001c0004t0027g0250 | 2 | HG01106.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.3779-2314G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49463870 | ||||||
chr10:49464093 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3779-2537C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464093 | ||||||
chr10:49464180 | C | T | 266 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(263): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.3779-2624G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464180 | ||||||
chr10:49464259 | C | T | 1 | a0009c0013t0013g0329 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3779-2703G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464259 | ||||||
chr10:49464343 | A | G | 1 | a0025c0032t0016g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3779-2787T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464343 | ||||||
chr10:49464344 | T | G | 1 | a0007c0011t0022g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3779-2788A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464344 | ||||||
chr10:49464555 | A | G | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.3779-2999T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464555 | ||||||
chr10:49464644 | T | G | 1 | a0001c0005t0003g0289 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3779-3088A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464644 | ||||||
chr10:49464743 | G | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3779-3187C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464743 | ||||||
chr10:49464744 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3779-3188G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464744 | ||||||
chr10:49464770 | C | T | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3779-3214G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49464770 | ||||||
chr10:49465054 | AC | A | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3779-3499delG | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465054 | ||||||
chr10:49465159 | C | T | 1 | a0001c0004t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3779-3603G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465159 | ||||||
chr10:49465176 | T | G | 3 | a0002c0007t0004g0063a0002c0007t0004g0064a0002c0007t0004g0065 | 3 | NA18945.hp2 NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.3779-3620A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465176 | ||||||
chr10:49465188 | G | T | 1 | a0007c0011t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3779-3632C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465188 | ||||||
chr10:49465332 | C | T | 128 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(125): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.3779-3776G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465332 | ||||||
chr10:49465337 | T | C | 78 | a0001c0001t0002g0168a0001c0001t0002g0186a0002c0002t0004g0007others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.3779-3781A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465337 | ||||||
chr10:49465571 | C | T | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3779-4015G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465571 | ||||||
chr10:49465751 | T | A | 1 | a0014c0016t0018g0035 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3779-4195A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465751 | ||||||
chr10:49465878 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3778+4304T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49465878 | ||||||
chr10:49466054 | C | G | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3778+4128G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49466054 | ||||||
chr10:49466367 | T | C | 2 | a0012c0018t0002g0224a0012c0018t0002g0225 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3778+3815A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49466367 | ||||||
chr10:49466548 | T | G | 1 | a0003c0003t0001g0264 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3778+3634A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49466548 | ||||||
chr10:49466612 | C | G | 1 | a0002c0002t0004g0082 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3778+3570G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49466612 | ||||||
chr10:49466732 | C | G | 1 | a0001c0009t0035g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3778+3450G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49466732 | ||||||
chr10:49466980 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3778+3202G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49466980 | ||||||
chr10:49467039 | C | A | 113 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(110): Show | 126 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.3778+3143G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467039 | ||||||
chr10:49467185 | C | T | 7 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(4): Show | 8 | HG01981.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3778+2997G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467185 | ||||||
chr10:49467199 | C | T | 1 | a0007c0011t0022g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3778+2983G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467199 | ||||||
chr10:49467283 | C | T | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3778+2899G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467283 | ||||||
chr10:49467346 | T | C | 1 | a0014c0016t0018g0035 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3778+2836A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467346 | ||||||
chr10:49467552 | A | G | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.3778+2630T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467552 | ||||||
chr10:49467692 | A | G | 2 | a0002c0002t0015g0055a0002c0002t0015g0056 | 2 | HG02523.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3778+2490T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467692 | ||||||
chr10:49467726 | C | G | 3 | a0002c0002t0006g0340a0002c0002t0020g0081a0002c0002t0037g0342 | 3 | HG00621.hp2 HG02074.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.3778+2456G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467726 | ||||||
chr10:49467878 | T | G | 127 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(124): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.3778+2304A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49467878 | ||||||
chr10:49468040 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3778+2142T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468040 | ||||||
chr10:49468119 | T | C | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.3778+2063A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468119 | ||||||
chr10:49468178 | T | C | 1 | a0002c0002t0039g0335 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3778+2004A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468178 | ||||||
chr10:49468295 | T | G | 7 | a0002c0007t0004g0066a0002c0007t0004g0068a0002c0007t0004g0069others(4): Show | 7 | HG01261.hp2 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.3778+1887A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468295 | ||||||
chr10:49468435 | C | T | 1 | a0007c0011t0022g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3778+1747G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468435 | ||||||
chr10:49468522 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3778+1660C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468522 | ||||||
chr10:49468701 | A | C | 3 | a0009c0013t0013g0034a0009c0013t0013g0329a0014c0016t0018g0035 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3778+1481T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468701 | ||||||
chr10:49468904 | T | C | 1 | a0001c0001t0002g0018 | 2 | HG00099.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3778+1278A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468904 | ||||||
chr10:49468983 | GA | G | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.3778+1198delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49468983 | ||||||
chr10:49469068 | G | A | 14 | a0001c0004t0001g0016a0001c0004t0001g0140a0001c0004t0001g0143others(11): Show | 15 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3778+1114C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469068 | ||||||
chr10:49469440 | A | G | 7 | a0001c0005t0003g0286a0001c0005t0003g0288a0001c0005t0003g0289others(4): Show | 7 | HG01099.hp1 HG01346.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3778+742T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469440 | ||||||
chr10:49469698 | A | C | 1 | a0011c0015t0004g0037 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3778+484T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469698 | ||||||
chr10:49469705 | T | C | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3778+477A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469705 | ||||||
chr10:49469770 | T | A | 2 | a0002c0007t0004g0071a0002c0007t0004g0073 | 2 | HG02083.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3778+412A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469770 | ||||||
chr10:49469896 | C | T | 1 | a0001c0005t0003g0269 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3778+286G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469896 | ||||||
chr10:49469905 | G | A | 2 | a0001c0004t0001g0140a0001c0004t0001g0145 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3778+277C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49469905 | ||||||
chr10:49470020 | G | A | 129 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(126): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.3778+162C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49470020 | ||||||
chr10:49470062 | G | C | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3778+120C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49470062 | ||||||
chr10:49470166 | G | A | 19 | a0002c0002t0005g0036a0002c0002t0005g0045a0002c0002t0005g0046others(16): Show | 19 | HG00438.hp2 HG00597.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.3778+16C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 18/20 | chr10 | 49470166 | ||||||
chr10:49470924 | G | A | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3071-35C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 17/20 | chr10 | 49470924 | ||||||
chr10:49470945 | T | C | 1 | a0001c0001t0002g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3070+30A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 17/20 | chr10 | 49470945 | ||||||
chr10:49471266 | C | T | 3 | a0005c0008t0001g0128a0005c0008t0001g0130a0005c0008t0001g0133 | 3 | HG02572.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2925-146G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/20 | chr10 | 49471266 | ||||||
chr10:49471350 | G | A | 1 | a0007c0011t0022g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2925-230C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/20 | chr10 | 49471350 | ||||||
chr10:49471408 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2925-288G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/20 | chr10 | 49471408 | ||||||
chr10:49471642 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2925-522G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/20 | chr10 | 49471642 | ||||||
chr10:49471775 | A | G | 1 | a0001c0001t0033g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2924+601T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/20 | chr10 | 49471775 | ||||||
chr10:49471835 | G | A | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2924+541C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 16/20 | chr10 | 49471835 | ||||||
chr10:49472531 | T | C | 1 | a0001c0009t0002g0167 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2830-61A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 15/20 | chr10 | 49472531 | ||||||
chr10:49472639 | A | C | 339 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(336): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.2830-169T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 15/20 | chr10 | 49472639 | ||||||
chr10:49472799 | T | C | 7 | a0003c0003t0001g0106a0003c0003t0001g0107a0003c0003t0001g0108others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2829+110A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 15/20 | chr10 | 49472799 | ||||||
chr10:49473111 | A | G | 18 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(15): Show | 22 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2710-83T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 14/20 | chr10 | 49473111 | ||||||
chr10:49473123 | G | T | 1 | a0001c0001t0002g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2710-95C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 14/20 | chr10 | 49473123 | ||||||
chr10:49473258 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2709+219C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 14/20 | chr10 | 49473258 | ||||||
chr10:49473433 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2709+44C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 14/20 | chr10 | 49473433 | ||||||
chr10:49473867 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2598+160A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 13/20 | chr10 | 49473867 | ||||||
chr10:49474476 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2383-234C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49474476 | ||||||
chr10:49474745 | T | C | 12 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(9): Show | 13 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2383-503A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49474745 | ||||||
chr10:49474751 | A | G | 49 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(46): Show | 57 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.2383-509T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49474751 | ||||||
chr10:49475044 | G | C | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2383-802C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475044 | ||||||
chr10:49475212 | C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(75): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2383-970G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475212 | ||||||
chr10:49475386 | T | C | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2382+829A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475386 | ||||||
chr10:49475392 | T | C | 45 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(42): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2382+823A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475392 | ||||||
chr10:49475394 | C | T | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2382+821G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475394 | ||||||
chr10:49475446 | G | A | 7 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2382+769C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475446 | ||||||
chr10:49475483 | G | T | 1 | a0004c0006t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2382+732C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475483 | ||||||
chr10:49475625 | G | A | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2382+590C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475625 | ||||||
chr10:49475762 | T | C | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2382+453A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475762 | ||||||
chr10:49475856 | T | C | 5 | a0001c0005t0003g0257a0001c0005t0003g0272a0001c0005t0003g0294others(2): Show | 5 | HG02155.hp2 NA18747.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2382+359A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475856 | ||||||
chr10:49475908 | C | T | 1 | a0001c0004t0001g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2382+307G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475908 | ||||||
chr10:49475927 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2382+288T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475927 | ||||||
chr10:49475957 | C | T | 1 | a0002c0002t0037g0342 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2382+258G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49475957 | ||||||
chr10:49476161 | C | T | 10 | a0001c0001t0002g0165a0001c0001t0002g0170a0001c0001t0002g0171others(7): Show | 10 | NA18747.hp2 NA18946.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.2382+54G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49476161 | ||||||
chr10:49476182 | A | G | 80 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(77): Show | 84 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2382+33T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 12/20 | chr10 | 49476182 | ||||||
chr10:49476562 | C | T | 2 | a0001c0001t0002g0173a0025c0032t0016g0155 | 2 | HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2287-252G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49476562 | ||||||
chr10:49476628 | C | T | 11 | a0001c0005t0003g0029a0001c0005t0003g0270a0001c0005t0003g0286others(8): Show | 12 | HG01099.hp1 HG01346.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2287-318G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49476628 | ||||||
chr10:49476660 | G | A | 1 | a0001c0004t0001g0151 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2287-350C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49476660 | ||||||
chr10:49476763 | T | C | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.2287-453A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49476763 | ||||||
chr10:49476797 | C | A | 4 | a0007c0011t0001g0253a0007c0011t0001g0255a0007c0011t0022g0090others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2287-487G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49476797 | ||||||
chr10:49477001 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2287-691A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477001 | ||||||
chr10:49477008 | G | A | 1 | a0002c0002t0004g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2287-698C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477008 | ||||||
chr10:49477131 | C | T | 12 | a0001c0005t0003g0027a0001c0005t0003g0256a0001c0005t0003g0257others(9): Show | 13 | HG01978.hp2 HG02071.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.2287-821G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477131 | ||||||
chr10:49477141 | G | A | 1 | a0003c0003t0001g0105 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2287-831C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477141 | ||||||
chr10:49477718 | G | A | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2286+636C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477718 | ||||||
chr10:49477810 | C | G | 1 | a0001c0004t0027g0250 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2286+544G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477810 | ||||||
chr10:49477926 | T | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2286+428A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477926 | ||||||
chr10:49477981 | T | C | 1 | a0002c0002t0004g0058 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2286+373A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49477981 | ||||||
chr10:49478207 | G | A | 1 | a0002c0002t0005g0085 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2286+147C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49478207 | ||||||
chr10:49478310 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2286+44T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 11/20 | chr10 | 49478310 | ||||||
chr10:49478508 | G | A | 3 | a0001c0001t0002g0005a0001c0001t0002g0229a0001c0001t0002g0230 | 5 | HG00280.hp2 HG01106.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.2170-38C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49478508 | ||||||
chr10:49478519 | G | A | 1 | a0005c0008t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2170-49C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49478519 | ||||||
chr10:49478554 | T | TA | 9 | a0001c0001t0002g0158a0001c0004t0001g0122a0001c0004t0001g0123others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2170-85dupT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49478554 | ||||||
chr10:49478554 | TA | T | 8 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237others(5): Show | 9 | HG02896.hp2 HG03209.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.2170-85delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49478554 | ||||||
chr10:49478565 | AAAG | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2170-98_2170-96del others(3): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49478565 | ||||||
chr10:49478940 | G | C | 1 | a0001c0001t0002g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2170-470C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49478940 | ||||||
chr10:49479045 | C | T | 6 | a0002c0002t0004g0057a0002c0002t0004g0058a0002c0002t0004g0059others(3): Show | 6 | NA18946.hp1 NA18970.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2170-575G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479045 | ||||||
chr10:49479076 | G | A | 1 | a0028c0034t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2170-606C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479076 | ||||||
chr10:49479087 | T | A | 1 | a0005c0008t0029g0139 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2170-617A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479087 | ||||||
chr10:49479188 | C | T | 4 | a0007c0011t0001g0253a0007c0011t0001g0255a0007c0011t0022g0090others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2170-718G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479188 | ||||||
chr10:49479350 | T | G | 1 | a0009c0013t0013g0034 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2170-880A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479350 | ||||||
chr10:49479351 | G | C | 1 | a0001c0009t0002g0164 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2170-881C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479351 | ||||||
chr10:49479506 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2170-1036A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479506 | ||||||
chr10:49479624 | A | G | 1 | a0021c0026t0030g0330 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2170-1154T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479624 | ||||||
chr10:49479675 | C | T | 76 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(73): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2170-1205G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479675 | ||||||
chr10:49479731 | G | C | 2 | a0003c0003t0001g0136a0003c0003t0001g0137 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2170-1261C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479731 | ||||||
chr10:49479880 | G | A | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2170-1410C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479880 | ||||||
chr10:49479950 | A | G | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2170-1480T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49479950 | ||||||
chr10:49480197 | C | T | 1 | a0001c0004t0007g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2170-1727G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480197 | ||||||
chr10:49480340 | G | T | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2170-1870C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480340 | ||||||
chr10:49480400 | A | G | 2 | a0006c0010t0008g0114a0006c0010t0008g0115 | 2 | HG01123.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2170-1930T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480400 | ||||||
chr10:49480609 | A | C | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.2169+2078T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480609 | ||||||
chr10:49480632 | A | G | 1 | a0007c0011t0028g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2169+2055T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480632 | ||||||
chr10:49480688 | A | G | 1 | a0003c0003t0001g0013 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2169+1999T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480688 | ||||||
chr10:49480695 | T | C | 2 | a0002c0012t0014g0323a0002c0012t0014g0325 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2169+1992A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480695 | ||||||
chr10:49480712 | C | T | 12 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(9): Show | 13 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2169+1975G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480712 | ||||||
chr10:49480774 | TTC | T | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2169+1911_2169+191 others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49480774 | ||||||
chr10:49481109 | G | A | 3 | a0001c0004t0001g0140a0001c0004t0001g0145a0001c0004t0001g0157 | 3 | HG02622.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2169+1578C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481109 | ||||||
chr10:49481133 | A | G | 1 | a0002c0002t0004g0074 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2169+1554T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481133 | ||||||
chr10:49481239 | T | G | 1 | a0001c0005t0003g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2169+1448A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481239 | ||||||
chr10:49481342 | A | T | 4 | a0001c0001t0002g0177a0001c0004t0001g0147a0002c0002t0017g0327others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2169+1345T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481342 | ||||||
chr10:49481352 | A | C | 3 | a0005c0008t0001g0128a0005c0008t0001g0130a0005c0008t0001g0133 | 3 | HG02572.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2169+1335T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481352 | ||||||
chr10:49481358 | TA | T | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2169+1328delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481358 | ||||||
chr10:49481463 | T | C | 12 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(9): Show | 13 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2169+1224A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481463 | ||||||
chr10:49481485 | T | C | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0040t0002g0245 | 3 | HG00735.hp2 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2169+1202A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481485 | ||||||
chr10:49481512 | A | C | 1 | a0024c0033t0003g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2169+1175T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481512 | ||||||
chr10:49481539 | C | A | 8 | a0001c0001t0002g0165a0001c0001t0002g0171a0001c0001t0002g0177others(5): Show | 8 | NA18951.hp1 NA18955.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.2169+1148G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481539 | ||||||
chr10:49481753 | C | A | 1 | a0001c0001t0002g0168 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2169+934G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481753 | ||||||
chr10:49481821 | C | T | 1 | a0002c0002t0006g0341 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2169+866G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481821 | ||||||
chr10:49481966 | C | A | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2169+721G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481966 | ||||||
chr10:49481971 | T | G | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2169+716A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49481971 | ||||||
chr10:49482022 | C | T | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2169+665G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482022 | ||||||
chr10:49482302 | T | C | 1 | a0001c0005t0003g0295 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2169+385A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482302 | ||||||
chr10:49482382 | C | T | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2169+305G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482382 | ||||||
chr10:49482425 | A | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0226 | 4 | HG01952.hp1 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.2169+262T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482425 | ||||||
chr10:49482473 | C | T | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2169+214G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482473 | ||||||
chr10:49482484 | T | C | 2 | a0004c0006t0001g0023a0004c0006t0001g0236 | 3 | NA18961.hp1 NA19068.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2169+203A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482484 | ||||||
chr10:49482539 | A | AT | 158 | a0001c0001t0002g0018a0001c0001t0002g0194a0001c0001t0002g0213others(155): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.2169+147dupA | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482539 | ||||||
chr10:49482539 | A | ATT | 14 | a0001c0004t0001g0122a0001c0004t0001g0124a0001c0004t0001g0125others(11): Show | 15 | HG01168.hp1 HG01192.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2169+146_2169+147d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482539 | ||||||
chr10:49482539 | A | ATTT | 29 | a0001c0004t0001g0123a0004c0006t0001g0022a0004c0006t0001g0023others(26): Show | 36 | HG01070.hp2 HG01071.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.2169+145_2169+147d others(5): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 10/20 | chr10 | 49482539 | ||||||
chr10:49482910 | A | G | 1 | a0007c0011t0001g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1993-47T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49482910 | ||||||
chr10:49482951 | T | C | 2 | a0002c0002t0004g0043a0002c0002t0004g0048 | 2 | NA18942.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1993-88A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49482951 | ||||||
chr10:49482963 | C | T | 128 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(125): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1993-100G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49482963 | ||||||
chr10:49482991 | C | T | 49 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(46): Show | 57 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1993-128G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49482991 | ||||||
chr10:49483113 | T | G | 7 | a0001c0004t0007g0025a0001c0004t0007g0238a0001c0004t0007g0239others(4): Show | 8 | HG01070.hp1 HG01074.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1992+233A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49483113 | ||||||
chr10:49483247 | A | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1992+99T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49483247 | ||||||
chr10:49483314 | T | C | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1992+32A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49483314 | ||||||
chr10:49483339 | G | A | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.1992+7C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 9/20 | chr10 | 49483339 | ||||||
chr10:49483686 | C | T | 1 | a0002c0002t0017g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1822-170G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49483686 | ||||||
chr10:49484001 | G | A | 3 | a0002c0002t0006g0343a0004c0006t0001g0307a0004c0006t0001g0316 | 3 | HG01070.hp2 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1822-485C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484001 | ||||||
chr10:49484062 | T | C | 1 | a0005c0008t0001g0014 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1822-546A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484062 | ||||||
chr10:49484263 | A | G | 17 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(14): Show | 20 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1822-747T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484263 | ||||||
chr10:49484278 | C | CA | 35 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(32): Show | 46 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1822-763dupT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484278 | ||||||
chr10:49484278 | CA | C | 79 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(76): Show | 83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1822-763delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484278 | ||||||
chr10:49484278 | CAAAAAAA others(7): Show |
C | 1 | a0003c0003t0001g0026 | 2 | NA18940.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1822-776_1822-763d others(16): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484278 | ||||||
chr10:49484279 | AAAAAAAA others(6): Show |
A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-776_1822-764d others(15): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484279 | ||||||
chr10:49484292 | GA | G | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1822-777delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484292 | ||||||
chr10:49484293 | A | G | 1 | a0002c0002t0040g0344 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1822-777T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484293 | ||||||
chr10:49484300 | A | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(74): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1822-784T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484300 | ||||||
chr10:49484670 | TTAGAGTC | T | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1822-1161_1822-115 others(11): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484670 | ||||||
chr10:49484678 | T | C | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1822-1162A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484678 | ||||||
chr10:49484724 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1822-1208G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484724 | ||||||
chr10:49484728 | A | G | 114 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(111): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1822-1212T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484728 | ||||||
chr10:49484751 | A | G | 6 | a0001c0005t0003g0257a0001c0005t0003g0272a0001c0005t0003g0294others(3): Show | 6 | HG02155.hp2 NA18747.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1822-1235T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484751 | ||||||
chr10:49484902 | G | A | 1 | a0001c0004t0007g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1822-1386C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484902 | ||||||
chr10:49484940 | C | T | 1 | a0001c0004t0007g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1822-1424G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49484940 | ||||||
chr10:49485007 | G | A | 1 | a0004c0006t0010g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1822-1491C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485007 | ||||||
chr10:49485080 | G | A | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1822-1564C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485080 | ||||||
chr10:49485304 | C | T | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1822-1788G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485304 | ||||||
chr10:49485335 | C | A | 1 | a0006c0010t0008g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1822-1819G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485335 | ||||||
chr10:49485535 | G | A | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1822-2019C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485535 | ||||||
chr10:49485571 | A | G | 1 | a0001c0005t0003g0284 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1822-2055T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485571 | ||||||
chr10:49485920 | T | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(74): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1822-2404A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49485920 | ||||||
chr10:49486171 | A | C | 1 | a0025c0032t0016g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1822-2655T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49486171 | ||||||
chr10:49486287 | C | G | 1 | a0003c0003t0001g0107 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1822-2771G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49486287 | ||||||
chr10:49486327 | T | C | 1 | a0013c0019t0002g0214 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1822-2811A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49486327 | ||||||
chr10:49486543 | G | A | 1 | a0004c0006t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1822-3027C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49486543 | ||||||
chr10:49486738 | T | C | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1822-3222A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49486738 | ||||||
chr10:49486948 | C | A | 1 | a0010c0017t0024g0259 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1822-3432G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49486948 | ||||||
chr10:49487034 | G | A | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1822-3518C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487034 | ||||||
chr10:49487054 | C | T | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1822-3538G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487054 | ||||||
chr10:49487186 | A | G | 1 | a0002c0002t0017g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1822-3670T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487186 | ||||||
chr10:49487562 | ACCAT | A | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1822-4050_1822-404 others(8): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487562 | ||||||
chr10:49487595 | C | T | 1 | a0001c0004t0027g0250 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1822-4079G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487595 | ||||||
chr10:49487677 | G | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1822-4161C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487677 | ||||||
chr10:49487896 | C | T | 1 | a0004c0006t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1822-4380G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49487896 | ||||||
chr10:49488035 | C | T | 1 | a0028c0034t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1822-4519G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488035 | ||||||
chr10:49488049 | C | T | 1 | a0003c0003t0001g0107 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1822-4533G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488049 | ||||||
chr10:49488198 | G | C | 2 | a0002c0002t0017g0120a0002c0002t0017g0327 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1822-4682C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488198 | ||||||
chr10:49488541 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1821+4576T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488541 | ||||||
chr10:49488642 | C | CT | 7 | a0002c0002t0004g0058a0004c0006t0001g0032a0004c0006t0001g0033others(4): Show | 9 | HG03486.hp1 NA18612.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1821+4474dupA | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488642 | ||||||
chr10:49488642 | CT | C | 61 | a0001c0001t0002g0192a0001c0001t0002g0195a0001c0001t0002g0234others(58): Show | 70 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1821+4474delA | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488642 | ||||||
chr10:49488643 | T | C | 1 | a0003c0003t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1821+4474A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488643 | ||||||
chr10:49488658 | T | A | 1 | a0001c0001t0002g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1821+4459A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488658 | ||||||
chr10:49488658 | TA | T | 4 | a0002c0002t0004g0041a0002c0002t0004g0043a0002c0002t0005g0050others(1): Show | 4 | NA18939.hp1 NA18942.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821+4458delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488658 | ||||||
chr10:49488659 | A | T | 74 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(71): Show | 78 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1821+4458T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488659 | ||||||
chr10:49488801 | T | C | 1 | a0001c0004t0007g0025 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1821+4316A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488801 | ||||||
chr10:49488823 | G | A | 1 | a0002c0002t0005g0088 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1821+4294C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488823 | ||||||
chr10:49488869 | C | T | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+4248G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49488869 | ||||||
chr10:49489543 | C | T | 2 | a0011c0015t0004g0037a0011c0015t0004g0038 | 2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1821+3574G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49489543 | ||||||
chr10:49489622 | C | G | 2 | a0001c0005t0003g0268a0001c0005t0003g0279 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1821+3495G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49489622 | ||||||
chr10:49489657 | G | A | 1 | a0028c0034t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1821+3460C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49489657 | ||||||
chr10:49489849 | C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0040t0002g0245 | 3 | HG00735.hp2 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+3268G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49489849 | ||||||
chr10:49490022 | A | C | 16 | a0001c0004t0001g0015a0001c0004t0001g0140a0001c0004t0001g0143others(13): Show | 18 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1821+3095T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490022 | ||||||
chr10:49490032 | G | T | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1821+3085C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490032 | ||||||
chr10:49490161 | T | C | 1 | a0001c0004t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1821+2956A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490161 | ||||||
chr10:49490271 | C | A | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1821+2846G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490271 | ||||||
chr10:49490357 | C | CT | 316 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(313): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1821+2759dupA | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490357 | ||||||
chr10:49490357 | C | CTT | 8 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237others(5): Show | 10 | HG01981.hp1 HG02293.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1821+2758_1821+275 others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490357 | ||||||
chr10:49490500 | G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1821+2617C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490500 | ||||||
chr10:49490635 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1821+2482C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490635 | ||||||
chr10:49490644 | C | T | 1 | a0005c0008t0001g0128 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1821+2473G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490644 | ||||||
chr10:49490648 | C | T | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1821+2469G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490648 | ||||||
chr10:49490650 | G | T | 1 | a0001c0001t0002g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1821+2467C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490650 | ||||||
chr10:49490651 | A | C | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1821+2466T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490651 | ||||||
chr10:49490672 | A | C | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1821+2445T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490672 | ||||||
chr10:49490682 | C | A | 1 | a0007c0011t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1821+2435G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49490682 | ||||||
chr10:49491135 | T | C | 5 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(2): Show | 6 | HG02630.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1821+1982A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491135 | ||||||
chr10:49491360 | T | A | 1 | a0001c0005t0003g0275 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1821+1757A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491360 | ||||||
chr10:49491376 | A | C | 1 | a0002c0002t0006g0343 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1821+1741T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491376 | ||||||
chr10:49491410 | A | G | 2 | a0001c0005t0003g0267a0001c0005t0003g0281 | 2 | HG00621.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1821+1707T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491410 | ||||||
chr10:49491444 | G | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1821+1673C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491444 | ||||||
chr10:49491722 | T | C | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1821+1395A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491722 | ||||||
chr10:49491790 | A | G | 76 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(73): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1821+1327T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491790 | ||||||
chr10:49491890 | A | G | 1 | a0002c0002t0009g0012 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1821+1227T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49491890 | ||||||
chr10:49492006 | T | C | 17 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(14): Show | 20 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1821+1111A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492006 | ||||||
chr10:49492142 | G | T | 4 | a0014c0016t0018g0035a0016c0028t0001g0091a0018c0024t0001g0322others(1): Show | 5 | HG01981.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821+975C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492142 | ||||||
chr10:49492219 | T | C | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1821+898A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492219 | ||||||
chr10:49492289 | C | T | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1821+828G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492289 | ||||||
chr10:49492295 | C | T | 1 | a0003c0003t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1821+822G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492295 | ||||||
chr10:49492319 | A | G | 1 | a0001c0040t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1821+798T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492319 | ||||||
chr10:49492363 | A | G | 1 | a0003c0003t0001g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1821+754T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492363 | ||||||
chr10:49492367 | T | A | 2 | a0002c0002t0004g0043a0002c0002t0004g0048 | 2 | NA18942.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1821+750A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492367 | ||||||
chr10:49492396 | G | A | 2 | a0001c0001t0002g0196a0001c0040t0002g0245 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+721C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492396 | ||||||
chr10:49492524 | C | T | 1 | a0002c0002t0006g0340 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1821+593G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492524 | ||||||
chr10:49492528 | G | A | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1821+589C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492528 | ||||||
chr10:49492544 | C | T | 1 | a0003c0003t0001g0013 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1821+573G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492544 | ||||||
chr10:49492566 | T | C | 1 | a0002c0002t0005g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1821+551A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492566 | ||||||
chr10:49492585 | C | T | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821+532G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492585 | ||||||
chr10:49492901 | A | G | 1 | a0002c0007t0004g0066 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1821+216T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492901 | ||||||
chr10:49492920 | G | T | 2 | a0002c0002t0009g0326a0002c0002t0009g0328 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1821+197C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49492920 | ||||||
chr10:49493091 | A | G | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+26T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49493091 | ||||||
chr10:49493093 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1821+24T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49493093 | ||||||
chr10:49493110 | G | A | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
splice_region_variant&intron_variant | LOW | c.1821+7C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 8/20 | chr10 | 49493110 | ||||||
chr10:49493372 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1686-120A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493372 | ||||||
chr10:49493550 | A | T | 1 | a0028c0034t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1686-298T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493550 | ||||||
chr10:49493684 | T | C | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1686-432A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493684 | ||||||
chr10:49493761 | G | T | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1686-509C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493761 | ||||||
chr10:49493769 | G | T | 1 | a0001c0005t0003g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1686-517C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493769 | ||||||
chr10:49493811 | T | A | 4 | a0007c0011t0001g0253a0007c0011t0001g0255a0007c0011t0022g0090others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686-559A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493811 | ||||||
chr10:49493872 | G | A | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1686-620C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493872 | ||||||
chr10:49493873 | A | G | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1686-621T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493873 | ||||||
chr10:49493881 | C | G | 2 | a0001c0001t0002g0004a0001c0001t0002g0226 | 4 | HG01952.hp1 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686-629G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493881 | ||||||
chr10:49493886 | C | T | 1 | a0003c0003t0001g0107 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1686-634G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493886 | ||||||
chr10:49493919 | G | T | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1686-667C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493919 | ||||||
chr10:49493920 | T | G | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1686-668A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493920 | ||||||
chr10:49493931 | G | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1686-679C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493931 | ||||||
chr10:49493956 | G | A | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1686-704C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49493956 | ||||||
chr10:49494001 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1686-749G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494001 | ||||||
chr10:49494144 | G | T | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1686-892C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494144 | ||||||
chr10:49494178 | G | A | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1686-926C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494178 | ||||||
chr10:49494329 | T | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1686-1077A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494329 | ||||||
chr10:49494422 | C | T | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1686-1170G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494422 | ||||||
chr10:49494479 | C | T | 1 | a0028c0034t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1686-1227G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494479 | ||||||
chr10:49494505 | T | G | 7 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1686-1253A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494505 | ||||||
chr10:49494536 | T | C | 1 | a0003c0003t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1686-1284A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494536 | ||||||
chr10:49494812 | A | ATAAGGAG others(3): Show |
1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1686-1570_1686-156 others(14): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494812 | ||||||
chr10:49494841 | C | T | 1 | a0001c0005t0003g0271 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1686-1589G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49494841 | ||||||
chr10:49495015 | G | A | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1686-1763C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495015 | ||||||
chr10:49495017 | C | T | 2 | a0002c0002t0017g0120a0002c0002t0017g0327 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1686-1765G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495017 | ||||||
chr10:49495077 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1686-1825C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495077 | ||||||
chr10:49495184 | G | A | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1686-1932C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495184 | ||||||
chr10:49495187 | G | A | 1 | a0002c0002t0037g0342 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1686-1935C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495187 | ||||||
chr10:49495276 | C | T | 1 | a0004c0006t0001g0315 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1686-2024G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495276 | ||||||
chr10:49495443 | C | T | 1 | a0001c0005t0003g0280 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1686-2191G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495443 | ||||||
chr10:49495549 | T | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(125): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1686-2297A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495549 | ||||||
chr10:49495587 | G | A | 109 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(106): Show | 121 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1686-2335C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495587 | ||||||
chr10:49495951 | C | G | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1686-2699G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495951 | ||||||
chr10:49495960 | T | C | 2 | a0001c0005t0003g0268a0001c0005t0003g0279 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1686-2708A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49495960 | ||||||
chr10:49496045 | C | G | 7 | a0001c0004t0007g0025a0001c0004t0007g0238a0001c0004t0007g0239others(4): Show | 8 | HG01070.hp1 HG01074.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1686-2793G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496045 | ||||||
chr10:49496100 | A | G | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1686-2848T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496100 | ||||||
chr10:49496152 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1686-2900G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496152 | ||||||
chr10:49496574 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1686-3322C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496574 | ||||||
chr10:49496637 | G | A | 43 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(40): Show | 49 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1686-3385C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496637 | ||||||
chr10:49496787 | G | A | 114 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(111): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1686-3535C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496787 | ||||||
chr10:49496810 | GAACAAAC others(1): Show |
G | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686-3566_1686-355 others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496810 | ||||||
chr10:49496991 | G | A | 42 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(39): Show | 48 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1685+3547C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49496991 | ||||||
chr10:49497048 | G | A | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1685+3490C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497048 | ||||||
chr10:49497193 | A | G | 2 | a0001c0005t0003g0270a0001c0005t0003g0290 | 2 | NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1685+3345T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497193 | ||||||
chr10:49497423 | T | G | 1 | a0002c0002t0004g0040 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1685+3115A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497423 | ||||||
chr10:49497558 | C | T | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1685+2980G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497558 | ||||||
chr10:49497574 | G | A | 1 | a0002c0002t0005g0050 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1685+2964C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497574 | ||||||
chr10:49497788 | C | T | 1 | a0001c0004t0001g0015 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1685+2750G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497788 | ||||||
chr10:49497988 | G | C | 1 | a0001c0004t0007g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1685+2550C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49497988 | ||||||
chr10:49498379 | G | C | 1 | a0003c0003t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1685+2159C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49498379 | ||||||
chr10:49498403 | G | A | 341 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(338): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1685+2135C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49498403 | ||||||
chr10:49498768 | A | G | 1 | a0005c0008t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1685+1770T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49498768 | ||||||
chr10:49498848 | G | A | 2 | a0025c0032t0016g0155a0029c0036t0016g0093 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1685+1690C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49498848 | ||||||
chr10:49498941 | G | A | 49 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(46): Show | 57 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1685+1597C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49498941 | ||||||
chr10:49499345 | G | A | 1 | a0002c0007t0004g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1685+1193C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499345 | ||||||
chr10:49499346 | A | G | 1 | a0004c0006t0001g0310 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1685+1192T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499346 | ||||||
chr10:49499514 | G | T | 1 | a0001c0001t0033g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1685+1024C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499514 | ||||||
chr10:49499644 | T | C | 1 | a0023c0027t0001g0248 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1685+894A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499644 | ||||||
chr10:49499645 | G | A | 1 | a0002c0007t0004g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1685+893C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499645 | ||||||
chr10:49499696 | T | C | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1685+842A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499696 | ||||||
chr10:49499807 | A | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1685+731T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499807 | ||||||
chr10:49499893 | A | G | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1685+645T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499893 | ||||||
chr10:49499898 | C | T | 1 | a0001c0001t0033g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1685+640G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499898 | ||||||
chr10:49499923 | TA | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1685+614delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49499923 | ||||||
chr10:49500014 | G | C | 1 | a0018c0024t0001g0322 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1685+524C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49500014 | ||||||
chr10:49500015 | C | T | 1 | a0018c0024t0001g0322 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1685+523G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49500015 | ||||||
chr10:49500240 | T | C | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0212others(2): Show | 5 | HG02165.hp2 NA18972.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1685+298A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 7/20 | chr10 | 49500240 | ||||||
chr10:49500827 | G | A | 1 | a0002c0007t0004g0065 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1527-131C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49500827 | ||||||
chr10:49501592 | C | T | 1 | a0003c0003t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1527-896G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49501592 | ||||||
chr10:49501765 | G | T | 1 | a0007c0011t0028g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1527-1069C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49501765 | ||||||
chr10:49501873 | T | C | 1 | a0003c0003t0001g0283 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1527-1177A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49501873 | ||||||
chr10:49501953 | C | T | 1 | a0006c0010t0008g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1527-1257G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49501953 | ||||||
chr10:49502077 | C | T | 322 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(319): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1527-1381G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502077 | ||||||
chr10:49502118 | A | T | 3 | a0002c0007t0004g0063a0002c0007t0004g0064a0002c0007t0004g0065 | 3 | NA18945.hp2 NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1527-1422T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502118 | ||||||
chr10:49502131 | G | A | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1527-1435C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502131 | ||||||
chr10:49502145 | T | C | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1527-1449A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502145 | ||||||
chr10:49502181 | T | C | 1 | a0002c0007t0004g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1527-1485A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502181 | ||||||
chr10:49502296 | C | T | 2 | a0002c0012t0014g0323a0002c0012t0014g0325 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1527-1600G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502296 | ||||||
chr10:49502314 | C | T | 1 | a0002c0002t0006g0343 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1527-1618G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502314 | ||||||
chr10:49502355 | C | T | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1527-1659G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502355 | ||||||
chr10:49502574 | G | A | 322 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(319): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1527-1878C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502574 | ||||||
chr10:49502597 | G | A | 3 | a0003c0003t0001g0013a0003c0003t0001g0136a0003c0003t0001g0137 | 4 | HG01884.hp1 HG02257.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1527-1901C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502597 | ||||||
chr10:49502609 | T | A | 1 | a0025c0032t0016g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1527-1913A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502609 | ||||||
chr10:49502806 | A | T | 137 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(134): Show | 153 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1527-2110T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502806 | ||||||
chr10:49502824 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1527-2128T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502824 | ||||||
chr10:49502953 | CA | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(75): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1527-2258delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502953 | ||||||
chr10:49502977 | T | C | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527-2281A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49502977 | ||||||
chr10:49503105 | T | C | 1 | a0003c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1527-2409A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503105 | ||||||
chr10:49503163 | A | G | 2 | a0001c0004t0001g0146a0001c0029t0001g0152 | 2 | HG01167.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1527-2467T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503163 | ||||||
chr10:49503223 | T | C | 1 | a0004c0023t0010g0309 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1527-2527A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503223 | ||||||
chr10:49503250 | G | T | 1 | a0005c0008t0029g0139 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1527-2554C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503250 | ||||||
chr10:49503394 | A | G | 42 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(39): Show | 48 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1526+2490T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503394 | ||||||
chr10:49503469 | A | T | 1 | a0001c0004t0001g0247 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1526+2415T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503469 | ||||||
chr10:49503510 | G | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1526+2374C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503510 | ||||||
chr10:49503523 | T | C | 17 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(14): Show | 20 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1526+2361A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503523 | ||||||
chr10:49503567 | C | T | 2 | a0002c0002t0004g0039a0002c0002t0004g0040 | 2 | NA19009.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1526+2317G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503567 | ||||||
chr10:49503734 | A | T | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1526+2150T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49503734 | ||||||
chr10:49504078 | C | A | 1 | a0001c0004t0001g0247 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1526+1806G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504078 | ||||||
chr10:49504127 | C | T | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1526+1757G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504127 | ||||||
chr10:49504192 | AAAG | A | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1526+1689_1526+169 others(7): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504192 | ||||||
chr10:49504206 | ACT | A | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1526+1676_1526+167 others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504206 | ||||||
chr10:49504264 | T | G | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1526+1620A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504264 | ||||||
chr10:49504389 | G | A | 2 | a0002c0002t0004g0039a0002c0002t0004g0040 | 2 | NA19009.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1526+1495C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504389 | ||||||
chr10:49504413 | T | G | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1526+1471A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504413 | ||||||
chr10:49504484 | A | G | 1 | a0002c0002t0009g0204 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1526+1400T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504484 | ||||||
chr10:49504603 | C | T | 1 | a0002c0002t0004g0042 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1526+1281G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504603 | ||||||
chr10:49504614 | G | A | 2 | a0007c0011t0022g0090a0007c0011t0028g0252 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1526+1270C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504614 | ||||||
chr10:49504789 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1526+1095A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504789 | ||||||
chr10:49504832 | C | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1526+1052G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504832 | ||||||
chr10:49504861 | G | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1526+1023C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504861 | ||||||
chr10:49504974 | C | A | 1 | a0001c0004t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1526+910G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49504974 | ||||||
chr10:49505013 | T | G | 50 | a0003c0003t0001g0002a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 58 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1526+871A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49505013 | ||||||
chr10:49505297 | T | C | 1 | a0001c0005t0003g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1526+587A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49505297 | ||||||
chr10:49505597 | A | G | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1526+287T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 6/20 | chr10 | 49505597 | ||||||
chr10:49506064 | T | G | 1 | a0001c0001t0019g0220 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1398-52A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506064 | ||||||
chr10:49506320 | G | A | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1398-308C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506320 | ||||||
chr10:49506389 | G | A | 30 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(27): Show | 38 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1398-377C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506389 | ||||||
chr10:49506412 | G | GATTTT | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1398-401_1398-400i others(7): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506412 | ||||||
chr10:49506634 | T | C | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1398-622A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506634 | ||||||
chr10:49506680 | A | T | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1398-668T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506680 | ||||||
chr10:49506810 | GA | G | 6 | a0002c0002t0004g0075a0003c0003t0001g0100a0007c0011t0022g0090others(3): Show | 8 | HG01243.hp2 HG02145.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1398-799delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506810 | ||||||
chr10:49506998 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1398-986A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49506998 | ||||||
chr10:49507149 | A | G | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1398-1137T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507149 | ||||||
chr10:49507186 | C | A | 4 | a0007c0011t0001g0253a0007c0011t0001g0255a0007c0011t0022g0090others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398-1174G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507186 | ||||||
chr10:49507226 | C | T | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1398-1214G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507226 | ||||||
chr10:49507403 | G | A | 1 | a0002c0002t0015g0055 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1398-1391C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507403 | ||||||
chr10:49507465 | C | A | 2 | a0004c0006t0001g0033a0004c0006t0001g0312 | 3 | NA18951.hp2 NA18954.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1398-1453G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507465 | ||||||
chr10:49507637 | G | A | 1 | a0001c0004t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1398-1625C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507637 | ||||||
chr10:49507670 | C | A | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0212others(2): Show | 5 | HG02165.hp2 NA18972.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1398-1658G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507670 | ||||||
chr10:49507724 | T | C | 1 | a0004c0006t0001g0314 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1398-1712A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507724 | ||||||
chr10:49507741 | A | T | 1 | a0002c0002t0004g0044 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1398-1729T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507741 | ||||||
chr10:49507920 | AGATATAT others(33): Show |
A | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1398-1948_1398-190 others(44): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49507920 | ||||||
chr10:49508142 | A | G | 1 | a0001c0004t0001g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1398-2130T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508142 | ||||||
chr10:49508146 | A | C | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0040t0002g0245 | 3 | HG00735.hp2 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1398-2134T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508146 | ||||||
chr10:49508294 | T | C | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1398-2282A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508294 | ||||||
chr10:49508393 | C | A | 1 | a0006c0010t0008g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1398-2381G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508393 | ||||||
chr10:49508576 | A | G | 1 | a0005c0008t0001g0014 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1398-2564T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508576 | ||||||
chr10:49508605 | T | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1398-2593A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508605 | ||||||
chr10:49508696 | G | A | 1 | a0002c0002t0004g0075 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1398-2684C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508696 | ||||||
chr10:49508808 | C | G | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1398-2796G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508808 | ||||||
chr10:49508836 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1398-2824C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508836 | ||||||
chr10:49508860 | A | G | 4 | a0002c0002t0006g0334a0002c0002t0006g0336a0002c0002t0006g0337others(1): Show | 4 | HG01891.hp1 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-2848T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49508860 | ||||||
chr10:49509008 | C | T | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1398-2996G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49509008 | ||||||
chr10:49509250 | G | T | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1398-3238C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49509250 | ||||||
chr10:49509540 | C | T | 137 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(134): Show | 153 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1398-3528G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49509540 | ||||||
chr10:49509624 | A | C | 1 | a0001c0001t0002g0171 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1398-3612T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49509624 | ||||||
chr10:49510035 | C | G | 2 | a0006c0010t0008g0114a0006c0010t0008g0115 | 2 | HG01123.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1398-4023G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49510035 | ||||||
chr10:49510082 | G | A | 1 | a0001c0009t0035g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1398-4070C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49510082 | ||||||
chr10:49510342 | G | A | 2 | a0002c0002t0017g0120a0002c0002t0017g0327 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1398-4330C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49510342 | ||||||
chr10:49510410 | C | T | 1 | a0002c0002t0005g0046 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1398-4398G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49510410 | ||||||
chr10:49510535 | C | T | 1 | a0002c0002t0005g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1398-4523G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49510535 | ||||||
chr10:49510879 | A | ACCCATAT others(336): Show |
1 | a0002c0002t0006g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1398-4868_1398-486 others(347): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49510879 | ||||||
chr10:49511011 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0006g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1398-5009_1398-500 others(14): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511011 | ||||||
chr10:49511011 | CA | C | 10 | a0001c0001t0002g0200a0002c0002t0004g0039a0002c0002t0004g0040others(7): Show | 10 | HG00609.hp2 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398-5000delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511011 | ||||||
chr10:49511048 | A | G | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1398-5036T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511048 | ||||||
chr10:49511183 | C | A | 1 | a0001c0005t0003g0292 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1398-5171G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511183 | ||||||
chr10:49511427 | CT | C | 317 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(314): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1398-5416delA | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511427 | ||||||
chr10:49511454 | T | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(125): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1398-5442A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511454 | ||||||
chr10:49511637 | G | A | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1398-5625C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511637 | ||||||
chr10:49511808 | T | G | 1 | a0001c0004t0001g0247 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1398-5796A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511808 | ||||||
chr10:49511836 | G | A | 1 | a0001c0004t0001g0247 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1398-5824C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511836 | ||||||
chr10:49511984 | T | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(338): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1398-5972A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511984 | ||||||
chr10:49511985 | G | A | 8 | a0002c0002t0004g0057a0002c0002t0004g0058a0002c0002t0004g0059others(5): Show | 8 | HG02523.hp2 NA18946.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1398-5973C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49511985 | ||||||
chr10:49512025 | G | T | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-6013C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512025 | ||||||
chr10:49512038 | G | A | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1398-6026C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512038 | ||||||
chr10:49512119 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1398-6107T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512119 | ||||||
chr10:49512346 | T | C | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1398-6334A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512346 | ||||||
chr10:49512510 | G | A | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1398-6498C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512510 | ||||||
chr10:49512512 | G | T | 1 | a0001c0005t0003g0280 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1398-6500C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512512 | ||||||
chr10:49512549 | C | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0226 | 4 | HG01952.hp1 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-6537G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512549 | ||||||
chr10:49512643 | A | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0163a0001c0001t0002g0195 | 4 | HG02056.hp1 NA18947.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398-6631T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512643 | ||||||
chr10:49512689 | A | G | 1 | a0016c0028t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1398-6677T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512689 | ||||||
chr10:49512697 | G | T | 2 | a0011c0015t0004g0037a0011c0015t0004g0038 | 2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1398-6685C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512697 | ||||||
chr10:49512862 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1398-6850C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512862 | ||||||
chr10:49512950 | T | C | 1 | a0002c0007t0004g0069 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1398-6938A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49512950 | ||||||
chr10:49513001 | C | T | 1 | a0001c0005t0003g0269 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1398-6989G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513001 | ||||||
chr10:49513079 | T | G | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1398-7067A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513079 | ||||||
chr10:49513142 | T | C | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1398-7130A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513142 | ||||||
chr10:49513277 | C | A | 1 | a0004c0006t0001g0319 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1398-7265G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513277 | ||||||
chr10:49513663 | T | G | 1 | a0003c0003t0001g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1398-7651A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513663 | ||||||
chr10:49513705 | G | A | 1 | a0007c0011t0022g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1398-7693C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513705 | ||||||
chr10:49513788 | C | T | 1 | a0004c0006t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1398-7776G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513788 | ||||||
chr10:49513853 | TCTC | T | 5 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(2): Show | 5 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-7844_1398-784 others(7): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513853 | ||||||
chr10:49513967 | T | C | 1 | a0002c0012t0014g0325 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1398-7955A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49513967 | ||||||
chr10:49514000 | A | C | 1 | a0001c0004t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398-7988T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514000 | ||||||
chr10:49514049 | C | T | 2 | a0003c0003t0001g0261a0003c0003t0001g0262 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1398-8037G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514049 | ||||||
chr10:49514062 | A | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398-8050T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514062 | ||||||
chr10:49514137 | A | G | 12 | a0001c0005t0003g0003a0001c0005t0003g0260a0001c0005t0003g0267others(9): Show | 16 | HG00621.hp1 HG03834.hp2 HG03927.hp2 others(13): Show |
intron_variant | MODIFIER | c.1398-8125T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514137 | ||||||
chr10:49514565 | T | C | 1 | a0001c0005t0003g0276 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1398-8553A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514565 | ||||||
chr10:49514779 | T | G | 42 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(39): Show | 48 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1398-8767A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514779 | ||||||
chr10:49514826 | G | C | 339 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(336): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1398-8814C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514826 | ||||||
chr10:49514912 | C | T | 2 | a0002c0002t0017g0120a0002c0002t0017g0327 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1398-8900G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514912 | ||||||
chr10:49514923 | A | C | 319 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(316): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1398-8911T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49514923 | ||||||
chr10:49515241 | C | T | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+8792G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515241 | ||||||
chr10:49515271 | A | T | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+8762T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515271 | ||||||
chr10:49515287 | T | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1397+8746A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515287 | ||||||
chr10:49515638 | G | A | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1397+8395C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515638 | ||||||
chr10:49515695 | G | A | 1 | a0001c0004t0027g0250 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1397+8338C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515695 | ||||||
chr10:49515750 | C | T | 1 | a0003c0003t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1397+8283G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515750 | ||||||
chr10:49515779 | G | C | 2 | a0002c0002t0017g0120a0002c0002t0017g0327 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1397+8254C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515779 | ||||||
chr10:49515970 | C | T | 341 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(338): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1397+8063G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49515970 | ||||||
chr10:49516270 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+7763G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49516270 | ||||||
chr10:49516320 | T | C | 1 | a0003c0003t0001g0277 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1397+7713A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49516320 | ||||||
chr10:49516637 | T | C | 1 | a0002c0007t0004g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1397+7396A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49516637 | ||||||
chr10:49517296 | A | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1397+6737T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517296 | ||||||
chr10:49517406 | A | C | 5 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(2): Show | 6 | HG02630.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+6627T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517406 | ||||||
chr10:49517440 | T | C | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1397+6593A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517440 | ||||||
chr10:49517478 | C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0207 | 2 | NA18747.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1397+6555G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517478 | ||||||
chr10:49517480 | T | G | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1397+6553A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517480 | ||||||
chr10:49517696 | C | T | 1 | a0001c0004t0001g0242 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1397+6337G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517696 | ||||||
chr10:49517763 | C | T | 1 | a0001c0001t0036g0233 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1397+6270G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517763 | ||||||
chr10:49517794 | T | A | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1397+6239A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517794 | ||||||
chr10:49517804 | A | C | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+6229T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517804 | ||||||
chr10:49517890 | T | A | 1 | a0003c0003t0001g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1397+6143A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517890 | ||||||
chr10:49517920 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1397+6113T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517920 | ||||||
chr10:49517938 | A | G | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+6095T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49517938 | ||||||
chr10:49518026 | G | A | 1 | a0001c0005t0003g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1397+6007C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518026 | ||||||
chr10:49518141 | G | A | 1 | a0001c0005t0003g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1397+5892C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518141 | ||||||
chr10:49518302 | C | T | 1 | a0001c0004t0001g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1397+5731G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518302 | ||||||
chr10:49518423 | C | T | 2 | a0002c0002t0009g0326a0002c0002t0009g0328 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1397+5610G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518423 | ||||||
chr10:49518547 | T | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+5486A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518547 | ||||||
chr10:49518562 | C | T | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1397+5471G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518562 | ||||||
chr10:49518655 | C | T | 1 | a0002c0002t0004g0043 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1397+5378G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518655 | ||||||
chr10:49518719 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+5314T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518719 | ||||||
chr10:49518812 | G | A | 1 | a0001c0004t0001g0247 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1397+5221C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518812 | ||||||
chr10:49518844 | T | C | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1397+5189A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49518844 | ||||||
chr10:49519101 | T | G | 2 | a0002c0002t0005g0078a0017c0020t0005g0060 | 2 | HG00597.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1397+4932A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519101 | ||||||
chr10:49519154 | G | A | 1 | a0002c0002t0004g0058 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1397+4879C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519154 | ||||||
chr10:49519185 | C | T | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1397+4848G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519185 | ||||||
chr10:49519243 | G | C | 11 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(8): Show | 12 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397+4790C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519243 | ||||||
chr10:49519310 | T | C | 83 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1397+4723A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519310 | ||||||
chr10:49519496 | C | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1397+4537G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519496 | ||||||
chr10:49519535 | C | G | 1 | a0001c0005t0003g0260 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1397+4498G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519535 | ||||||
chr10:49519587 | G | A | 2 | a0001c0005t0025g0156a0002c0002t0004g0042 | 2 | HG00408.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1397+4446C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519587 | ||||||
chr10:49519603 | G | A | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1397+4430C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519603 | ||||||
chr10:49519636 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1397+4397C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519636 | ||||||
chr10:49519651 | G | A | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1397+4382C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519651 | ||||||
chr10:49519675 | T | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+4358A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519675 | ||||||
chr10:49519741 | C | T | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1397+4292G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519741 | ||||||
chr10:49519848 | G | A | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1397+4185C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519848 | ||||||
chr10:49519894 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1397+4139A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519894 | ||||||
chr10:49519905 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+4128G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519905 | ||||||
chr10:49519939 | C | T | 1 | a0001c0004t0001g0151 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1397+4094G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49519939 | ||||||
chr10:49520209 | T | G | 1 | a0002c0002t0009g0012 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1397+3824A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49520209 | ||||||
chr10:49520258 | C | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+3775G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49520258 | ||||||
chr10:49520281 | A | G | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1397+3752T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49520281 | ||||||
chr10:49520325 | C | A | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1397+3708G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49520325 | ||||||
chr10:49520374 | T | C | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1397+3659A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49520374 | ||||||
chr10:49520926 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+3107T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49520926 | ||||||
chr10:49521150 | T | C | 3 | a0003c0003t0001g0010a0003c0003t0001g0098a0003c0003t0001g0104 | 4 | HG02698.hp1 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+2883A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521150 | ||||||
chr10:49521239 | G | A | 1 | a0002c0002t0006g0341 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1397+2794C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521239 | ||||||
chr10:49521337 | T | C | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+2696A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521337 | ||||||
chr10:49521363 | C | T | 1 | a0001c0004t0007g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1397+2670G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521363 | ||||||
chr10:49521368 | C | T | 76 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(73): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1397+2665G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521368 | ||||||
chr10:49521518 | G | A | 1 | a0001c0005t0003g0298 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1397+2515C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521518 | ||||||
chr10:49521629 | T | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0194 | 2 | NA19067.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1397+2404A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521629 | ||||||
chr10:49521720 | A | G | 1 | a0001c0009t0002g0017 | 2 | HG00558.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1397+2313T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521720 | ||||||
chr10:49521738 | C | T | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1397+2295G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521738 | ||||||
chr10:49521811 | AG | A | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1397+2221delC | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521811 | ||||||
chr10:49521814 | G | A | 1 | a0002c0002t0006g0340 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1397+2219C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521814 | ||||||
chr10:49521815 | C | T | 2 | a0007c0011t0022g0090a0007c0011t0028g0252 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1397+2218G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521815 | ||||||
chr10:49521857 | C | G | 1 | a0007c0011t0028g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1397+2176G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521857 | ||||||
chr10:49521858 | G | A | 1 | a0001c0005t0003g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1397+2175C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49521858 | ||||||
chr10:49522134 | T | C | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1397+1899A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522134 | ||||||
chr10:49522205 | A | G | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1397+1828T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522205 | ||||||
chr10:49522312 | T | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+1721A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522312 | ||||||
chr10:49522370 | T | C | 1 | a0001c0005t0003g0280 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1397+1663A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522370 | ||||||
chr10:49522384 | G | A | 1 | a0001c0004t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1397+1649C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522384 | ||||||
chr10:49522478 | A | G | 1 | a0016c0028t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1397+1555T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522478 | ||||||
chr10:49522535 | A | G | 1 | a0002c0002t0006g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1397+1498T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522535 | ||||||
chr10:49522679 | A | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+1354T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522679 | ||||||
chr10:49522736 | G | T | 1 | a0016c0028t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1397+1297C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522736 | ||||||
chr10:49522983 | C | T | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1397+1050G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49522983 | ||||||
chr10:49523114 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1397+919C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523114 | ||||||
chr10:49523143 | G | A | 2 | a0001c0038t0002g0184a0022c0039t0002g0185 | 2 | NA18971.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1397+890C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523143 | ||||||
chr10:49523411 | T | A | 1 | a0001c0005t0003g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1397+622A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523411 | ||||||
chr10:49523580 | C | G | 1 | a0004c0006t0001g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1397+453G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523580 | ||||||
chr10:49523581 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1397+452G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523581 | ||||||
chr10:49523687 | T | C | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+346A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523687 | ||||||
chr10:49523727 | T | G | 2 | a0008c0014t0003g0028a0008c0014t0003g0282 | 3 | NA18953.hp2 NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1397+306A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523727 | ||||||
chr10:49523758 | G | C | 1 | a0002c0002t0004g0042 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1397+275C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523758 | ||||||
chr10:49523796 | C | T | 1 | a0018c0024t0001g0322 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1397+237G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523796 | ||||||
chr10:49523802 | C | G | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+231G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523802 | ||||||
chr10:49523838 | T | C | 1 | a0003c0003t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1397+195A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523838 | ||||||
chr10:49523839 | G | A | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1397+194C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523839 | ||||||
chr10:49523874 | C | G | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1397+159G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523874 | ||||||
chr10:49523939 | T | C | 1 | a0003c0003t0001g0283 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1397+94A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 5/20 | chr10 | 49523939 | ||||||
chr10:49524804 | G | A | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.653-27C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49524804 | ||||||
chr10:49524826 | G | A | 1 | a0024c0033t0003g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.653-49C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49524826 | ||||||
chr10:49525029 | C | A | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.653-252G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525029 | ||||||
chr10:49525047 | T | C | 1 | a0002c0002t0040g0344 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.653-270A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525047 | ||||||
chr10:49525139 | C | T | 1 | a0003c0003t0001g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.653-362G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525139 | ||||||
chr10:49525181 | T | C | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.653-404A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525181 | ||||||
chr10:49525235 | G | GAA | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-460_653-459dup others(2): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525235 | ||||||
chr10:49525246 | A | G | 5 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(2): Show | 6 | HG02630.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-469T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525246 | ||||||
chr10:49525281 | A | G | 2 | a0001c0009t0002g0017a0001c0009t0002g0189 | 3 | HG00558.hp2 NA18984.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.653-504T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525281 | ||||||
chr10:49525332 | C | T | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-555G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525332 | ||||||
chr10:49525375 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.653-598C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525375 | ||||||
chr10:49525494 | A | G | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-717T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525494 | ||||||
chr10:49525650 | T | C | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.653-873A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525650 | ||||||
chr10:49525767 | TAACAG | T | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-995_653-991del others(5): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525767 | ||||||
chr10:49525823 | G | A | 1 | a0024c0033t0003g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.653-1046C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525823 | ||||||
chr10:49525828 | C | G | 1 | a0004c0006t0001g0319 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.653-1051G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525828 | ||||||
chr10:49525857 | C | T | 138 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(135): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.653-1080G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525857 | ||||||
chr10:49525933 | C | G | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.653-1156G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525933 | ||||||
chr10:49525956 | ATCCTTAC others(12): Show |
A | 1 | a0002c0002t0006g0341 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.653-1198_653-1180d others(21): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525956 | ||||||
chr10:49525958 | C | T | 2 | a0025c0032t0016g0155a0029c0036t0016g0093 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.653-1181G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525958 | ||||||
chr10:49525971 | T | A | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.653-1194A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49525971 | ||||||
chr10:49526079 | TTTTATTT others(15): Show |
T | 1 | a0002c0002t0038g0339 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.653-1324_653-1303d others(24): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526079 | ||||||
chr10:49526085 | TTATATTT others(29): Show |
T | 1 | a0002c0007t0004g0071 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.653-1344_653-1309d others(38): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526085 | ||||||
chr10:49526088 | T | C | 5 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(2): Show | 5 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1311A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526088 | ||||||
chr10:49526089 | ATTTATAT others(19): Show |
A | 4 | a0002c0002t0004g0051a0002c0002t0004g0079a0002c0002t0005g0036others(1): Show | 4 | HG03669.hp1 NA18954.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1338_653-1313d others(28): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526089 | ||||||
chr10:49526091 | T | A | 1 | a0002c0002t0020g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.653-1314A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526091 | ||||||
chr10:49526091 | TTATATAT others(21): Show |
T | 7 | a0002c0002t0004g0049a0002c0002t0005g0050a0002c0002t0005g0084others(4): Show | 7 | HG00438.hp2 HG01891.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-1342_653-1315d others(30): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526091 | ||||||
chr10:49526091 | TTATATAT others(23): Show |
T | 13 | a0002c0002t0004g0008a0002c0002t0004g0043a0002c0002t0004g0044others(10): Show | 14 | HG01981.hp2 HG02071.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.653-1344_653-1315d others(32): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526091 | ||||||
chr10:49526091 | TTATATAT others(25): Show |
T | 26 | a0002c0002t0004g0007a0002c0002t0004g0039a0002c0002t0004g0040others(23): Show | 28 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.653-1346_653-1315d others(34): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526091 | ||||||
chr10:49526091 | TTATATAT others(35): Show |
T | 1 | a0002c0002t0006g0343 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.653-1356_653-1315d others(44): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526091 | ||||||
chr10:49526091 | TTATATAT others(41): Show |
T | 3 | a0002c0002t0009g0012a0002c0002t0009g0326a0002c0002t0009g0328 | 4 | HG00642.hp1 HG00741.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1362_653-1315d others(50): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526091 | ||||||
chr10:49526092 | TATATATT others(10): Show |
T | 1 | a0002c0002t0004g0059 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.653-1332_653-1316d others(19): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526092 | ||||||
chr10:49526093 | ATATATTT others(17): Show |
A | 4 | a0002c0002t0004g0053a0002c0002t0004g0054a0002c0002t0015g0055others(1): Show | 4 | HG00609.hp2 HG02165.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1340_653-1317d others(26): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526093 | ||||||
chr10:49526095 | ATATTTAT others(15): Show |
A | 5 | a0002c0002t0004g0057a0002c0002t0004g0058a0002c0002t0004g0086others(2): Show | 5 | HG02074.hp1 HG02717.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1340_653-1319d others(24): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526095 | ||||||
chr10:49526097 | ATTTATAT others(3): Show |
A | 2 | a0002c0002t0006g0338a0002c0007t0004g0073 | 2 | HG02083.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.653-1330_653-1321d others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526097 | ||||||
chr10:49526097 | ATTTATAT others(11): Show |
A | 2 | a0002c0002t0004g0087a0002c0002t0039g0335 | 2 | HG02451.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.653-1338_653-1321d others(20): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526097 | ||||||
chr10:49526099 | T | A | 6 | a0002c0002t0004g0089a0002c0002t0006g0336a0002c0002t0006g0337others(3): Show | 6 | HG00621.hp2 HG03130.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-1322A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526099 | ||||||
chr10:49526099 | TTATATAT others(23): Show |
T | 1 | a0005c0008t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.653-1352_653-1323d others(32): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526099 | ||||||
chr10:49526099 | TTATATAT others(29): Show |
T | 1 | a0005c0008t0001g0128 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.653-1358_653-1323d others(38): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526099 | ||||||
chr10:49526103 | ATATTTAT others(7): Show |
A | 1 | a0002c0002t0004g0089 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.653-1340_653-1327d others(16): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526103 | ||||||
chr10:49526105 | ATTTATAT others(5): Show |
A | 5 | a0002c0002t0006g0336a0002c0002t0006g0337a0002c0002t0006g0341others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1340_653-1329d others(14): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526105 | ||||||
chr10:49526107 | T | A | 8 | a0002c0002t0006g0340a0002c0002t0017g0120a0002c0002t0017g0327others(5): Show | 8 | HG00621.hp2 HG02074.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-1330A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526107 | T | TTA | 3 | a0003c0003t0001g0103a0003c0003t0001g0104a0003c0003t0001g0111 | 3 | HG00735.hp1 HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.653-1332_653-1331d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526107 | T | TTATA | 4 | a0003c0003t0001g0011a0003c0003t0001g0105a0003c0003t0001g0106others(1): Show | 5 | HG01261.hp1 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1334_653-1331d others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526107 | T | TTATATAT others(3): Show |
3 | a0003c0003t0001g0135a0003c0003t0001g0136a0003c0003t0001g0142 | 3 | HG02257.hp2 HG03942.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.653-1331_653-1330i others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526107 | T | TTATATAT others(5): Show |
1 | a0003c0003t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653-1331_653-1330i others(14): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526107 | TTATATAT others(17): Show |
T | 1 | a0005c0008t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.653-1354_653-1331d others(26): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526107 | TTATATAT others(31): Show |
T | 1 | a0025c0032t0016g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.653-1368_653-1331d others(40): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526107 | ||||||
chr10:49526109 | A | T | 4 | a0007c0011t0001g0253a0007c0011t0001g0255a0007c0011t0022g0090others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1332T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526109 | ||||||
chr10:49526111 | ATATTTT | A | 2 | a0002c0002t0017g0327a0005c0008t0001g0014 | 3 | HG01069.hp1 HG01071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.653-1340_653-1335d others(8): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526111 | ||||||
chr10:49526113 | ATT | A | 7 | a0003c0003t0001g0094a0003c0003t0001g0095a0003c0003t0001g0096others(4): Show | 7 | HG00140.hp2 HG00738.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-1338_653-1337d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526113 | ||||||
chr10:49526115 | T | A | 30 | a0002c0002t0006g0338a0002c0002t0006g0340a0002c0002t0017g0120others(27): Show | 33 | HG00621.hp2 HG00735.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.653-1338A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | T | TTATATAT others(9): Show |
1 | a0001c0040t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.653-1339_653-1338i others(18): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | T | TTATATAT others(15): Show |
1 | a0003c0003t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.653-1339_653-1338i others(24): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | T | TTATATAT others(35): Show |
1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.653-1339_653-1338i others(44): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTA | T | 8 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0004t0001g0247others(5): Show | 8 | HG01069.hp2 HG01123.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-1342_653-1339d others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(3): Show |
T | 2 | a0001c0001t0002g0197a0001c0004t0001g0125 | 2 | HG00735.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.653-1348_653-1339d others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(7): Show |
T | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1352_653-1339d others(16): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(9): Show |
T | 1 | a0018c0024t0001g0322 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.653-1354_653-1339d others(18): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(11): Show |
T | 3 | a0009c0013t0013g0034a0009c0013t0013g0329a0014c0016t0018g0035 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1356_653-1339d others(20): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(13): Show |
T | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.653-1358_653-1339d others(22): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(17): Show |
T | 1 | a0001c0001t0002g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.653-1362_653-1339d others(26): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(19): Show |
T | 5 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(2): Show | 5 | HG01981.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1364_653-1339d others(28): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(21): Show |
T | 91 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(88): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.653-1366_653-1339d others(30): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(23): Show |
T | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.653-1368_653-1339d others(32): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526115 | TTTTATAT others(25): Show |
T | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.653-1370_653-1339d others(34): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526115 | ||||||
chr10:49526117 | T | A | 43 | a0001c0040t0002g0245a0002c0002t0004g0087a0002c0002t0006g0338others(40): Show | 46 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.653-1340A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | T | TATATATA others(4): Show |
1 | a0007c0011t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.653-1341_653-1340i others(13): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | T | TTA | 4 | a0001c0004t0001g0244a0001c0004t0007g0239a0001c0004t0007g0240others(1): Show | 4 | HG01109.hp2 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1342_653-1341d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | T | TTATATAT others(3): Show |
1 | a0007c0011t0001g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.653-1350_653-1341d others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | T | TTATATAT others(9): Show |
1 | a0001c0004t0001g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653-1356_653-1341d others(18): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | TTATATAT others(1): Show |
T | 3 | a0001c0004t0001g0124a0001c0004t0001g0300a0023c0027t0001g0248 | 3 | HG01192.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.653-1348_653-1341d others(10): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | TTATATAT others(3): Show |
T | 2 | a0001c0004t0001g0122a0001c0004t0001g0123 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.653-1350_653-1341d others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | TTATATAT others(5): Show |
T | 1 | a0001c0004t0001g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.653-1352_653-1341d others(14): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | TTATATAT others(7): Show |
T | 1 | a0001c0004t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.653-1354_653-1341d others(16): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | TTATATAT others(19): Show |
T | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.653-1366_653-1341d others(28): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526117 | TTATATAT others(21): Show |
T | 54 | a0001c0001t0002g0168a0001c0005t0003g0003a0001c0005t0003g0027others(51): Show | 64 | HG00597.hp2 HG00621.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.653-1368_653-1341d others(30): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526117 | ||||||
chr10:49526139 | A | T | 1 | a0018c0024t0001g0322 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.653-1362T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526139 | ||||||
chr10:49526141 | A | T | 3 | a0009c0013t0013g0034a0009c0013t0013g0329a0014c0016t0018g0035 | 5 | HG01243.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1364T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526141 | ||||||
chr10:49526143 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.653-1366T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526143 | ||||||
chr10:49526155 | A | ATCTATCT others(3): Show |
1 | a0003c0003t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.653-1379_653-1378i others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526155 | ||||||
chr10:49526159 | A | C | 1 | a0003c0003t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.653-1382T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526159 | ||||||
chr10:49526203 | A | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.653-1426T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526203 | ||||||
chr10:49526235 | G | T | 1 | a0003c0003t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.653-1458C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526235 | ||||||
chr10:49526310 | T | C | 1 | a0009c0013t0013g0329 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.653-1533A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526310 | ||||||
chr10:49526316 | C | CT | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.653-1540dupA | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526316 | ||||||
chr10:49526362 | T | C | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1585A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526362 | ||||||
chr10:49526379 | T | C | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.653-1602A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526379 | ||||||
chr10:49526630 | T | A | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.652+1787A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526630 | ||||||
chr10:49526737 | T | C | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.652+1680A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526737 | ||||||
chr10:49526816 | G | A | 138 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(135): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.652+1601C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526816 | ||||||
chr10:49526886 | A | G | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.652+1531T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49526886 | ||||||
chr10:49527002 | C | A | 1 | a0002c0002t0004g0059 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.652+1415G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527002 | ||||||
chr10:49527094 | G | A | 1 | a0002c0002t0009g0012 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.652+1323C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527094 | ||||||
chr10:49527118 | A | G | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.652+1299T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527118 | ||||||
chr10:49527275 | C | T | 1 | a0001c0001t0002g0169 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.652+1142G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527275 | ||||||
chr10:49527351 | A | G | 1 | a0009c0013t0013g0034 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.652+1066T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527351 | ||||||
chr10:49527501 | C | G | 1 | a0001c0004t0001g0015 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.652+916G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527501 | ||||||
chr10:49527504 | G | A | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.652+913C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527504 | ||||||
chr10:49527572 | G | A | 31 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(28): Show | 39 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.652+845C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527572 | ||||||
chr10:49527589 | C | A | 138 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(135): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.652+828G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527589 | ||||||
chr10:49527606 | C | T | 3 | a0004c0006t0001g0303a0004c0006t0001g0313a0004c0006t0001g0314 | 3 | NA18994.hp1 NA18999.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.652+811G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49527606 | ||||||
chr10:49528014 | T | C | 5 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(2): Show | 6 | HG02630.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.652+403A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528014 | ||||||
chr10:49528034 | G | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.652+383C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528034 | ||||||
chr10:49528071 | G | A | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+346C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528071 | ||||||
chr10:49528109 | T | C | 2 | a0002c0002t0005g0078a0017c0020t0005g0060 | 2 | HG00597.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.652+308A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528109 | ||||||
chr10:49528136 | C | T | 1 | a0001c0004t0001g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.652+281G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528136 | ||||||
chr10:49528147 | T | C | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.652+270A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528147 | ||||||
chr10:49528274 | T | C | 3 | a0001c0001t0002g0213a0001c0001t0002g0222a0001c0001t0002g0223 | 3 | NA18941.hp2 NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.652+143A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528274 | ||||||
chr10:49528282 | A | T | 78 | a0002c0002t0004g0007a0002c0002t0004g0008a0002c0002t0004g0039others(75): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.652+135T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 4/20 | chr10 | 49528282 | ||||||
chr10:49528738 | G | C | 1 | a0001c0004t0001g0151 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.544-213C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49528738 | ||||||
chr10:49528754 | C | A | 1 | a0002c0002t0017g0327 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.544-229G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49528754 | ||||||
chr10:49528774 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.544-249G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49528774 | ||||||
chr10:49528933 | A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(75): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.544-408T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49528933 | ||||||
chr10:49529067 | C | T | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.544-542G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529067 | ||||||
chr10:49529096 | C | T | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.544-571G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529096 | ||||||
chr10:49529144 | G | T | 1 | a0002c0002t0005g0036 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.544-619C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529144 | ||||||
chr10:49529161 | C | A | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.544-636G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529161 | ||||||
chr10:49529235 | G | C | 1 | a0007c0011t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-710C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529235 | ||||||
chr10:49529352 | C | G | 1 | a0016c0028t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.544-827G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529352 | ||||||
chr10:49529398 | T | A | 1 | a0002c0002t0005g0036 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.544-873A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529398 | ||||||
chr10:49529399 | A | G | 1 | a0002c0002t0005g0036 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.544-874T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529399 | ||||||
chr10:49529496 | T | C | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.544-971A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529496 | ||||||
chr10:49529761 | G | A | 1 | a0023c0027t0001g0248 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.543+959C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529761 | ||||||
chr10:49529849 | T | C | 12 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(9): Show | 13 | HG01192.hp2 HG01884.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.543+871A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529849 | ||||||
chr10:49529938 | T | C | 1 | a0005c0008t0029g0139 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.543+782A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529938 | ||||||
chr10:49529968 | G | A | 2 | a0004c0006t0001g0310a0004c0006t0001g0311 | 2 | HG01934.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.543+752C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49529968 | ||||||
chr10:49530002 | G | T | 2 | a0007c0011t0022g0090a0007c0011t0028g0252 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.543+718C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530002 | ||||||
chr10:49530101 | G | A | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.543+619C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530101 | ||||||
chr10:49530199 | C | T | 1 | a0002c0007t0004g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.543+521G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530199 | ||||||
chr10:49530272 | C | A | 1 | a0016c0028t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.543+448G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530272 | ||||||
chr10:49530287 | T | C | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+433A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530287 | ||||||
chr10:49530318 | C | T | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.543+402G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530318 | ||||||
chr10:49530353 | A | G | 1 | a0004c0006t0001g0302 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.543+367T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530353 | ||||||
chr10:49530401 | T | C | 3 | a0001c0005t0003g0288a0001c0005t0003g0289a0001c0005t0003g0297 | 3 | HG01099.hp1 HG01346.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.543+319A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530401 | ||||||
chr10:49530410 | T | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+310A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530410 | ||||||
chr10:49530443 | G | A | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.543+277C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530443 | ||||||
chr10:49530515 | T | C | 1 | a0001c0001t0002g0021 | 2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.543+205A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 3/20 | chr10 | 49530515 | ||||||
chr10:49531035 | G | A | 1 | a0002c0002t0006g0341 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.423-195C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531035 | ||||||
chr10:49531070 | A | G | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.423-230T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531070 | ||||||
chr10:49531164 | G | A | 15 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(12): Show | 17 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.423-324C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531164 | ||||||
chr10:49531212 | G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.423-372C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531212 | ||||||
chr10:49531217 | C | G | 52 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(49): Show | 62 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.423-377G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531217 | ||||||
chr10:49531253 | A | T | 1 | a0023c0027t0001g0248 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.423-413T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531253 | ||||||
chr10:49531264 | T | C | 1 | a0007c0011t0028g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.423-424A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531264 | ||||||
chr10:49531282 | G | A | 3 | a0001c0001t0002g0195a0009c0013t0013g0034a0009c0013t0013g0329 | 4 | HG01243.hp2 HG02145.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-442C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531282 | ||||||
chr10:49531286 | A | G | 1 | a0007c0011t0028g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.423-446T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531286 | ||||||
chr10:49531322 | TACAGC | T | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.423-487_423-483del others(5): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531322 | ||||||
chr10:49531511 | C | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.423-671G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531511 | ||||||
chr10:49531728 | T | C | 5 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(2): Show | 5 | HG00735.hp2 HG01243.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.422+815A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531728 | ||||||
chr10:49531869 | C | T | 18 | a0001c0001t0002g0226a0001c0004t0001g0015a0001c0004t0001g0016others(15): Show | 21 | HG01167.hp1 HG01243.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.422+674G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531869 | ||||||
chr10:49531870 | G | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.422+673C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531870 | ||||||
chr10:49531914 | C | T | 31 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(28): Show | 39 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.422+629G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531914 | ||||||
chr10:49531917 | C | T | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.422+626G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49531917 | ||||||
chr10:49532097 | A | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.422+446T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49532097 | ||||||
chr10:49532125 | G | A | 1 | a0002c0002t0037g0342 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.422+418C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49532125 | ||||||
chr10:49532216 | G | T | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+327C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 2/20 | chr10 | 49532216 | ||||||
chr10:49533037 | A | G | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-14-59T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533037 | ||||||
chr10:49533134 | G | A | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-14-156C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533134 | ||||||
chr10:49533205 | A | C | 28 | a0004c0006t0001g0022a0004c0006t0001g0023a0004c0006t0001g0030others(25): Show | 36 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-14-227T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533205 | ||||||
chr10:49533358 | T | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-380A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533358 | ||||||
chr10:49533383 | T | C | 138 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(135): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.-14-405A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533383 | ||||||
chr10:49533393 | G | A | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-14-415C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533393 | ||||||
chr10:49533448 | A | G | 1 | a0001c0009t0002g0167 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-14-470T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533448 | ||||||
chr10:49533531 | C | T | 2 | a0007c0011t0001g0253a0007c0011t0001g0255 | 2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-14-553G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533531 | ||||||
chr10:49533537 | C | T | 1 | a0004c0006t0001g0312 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-14-559G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533537 | ||||||
chr10:49533571 | C | T | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-593G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533571 | ||||||
chr10:49533617 | GATA | G | 4 | a0007c0011t0001g0253a0007c0011t0001g0255a0007c0011t0022g0090others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-642_-14-640del others(3): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533617 | ||||||
chr10:49533645 | T | C | 31 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(28): Show | 39 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-667A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533645 | ||||||
chr10:49533716 | T | A | 1 | a0002c0002t0004g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-14-738A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533716 | ||||||
chr10:49533809 | T | C | 2 | a0012c0018t0002g0224a0012c0018t0002g0225 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-14-831A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533809 | ||||||
chr10:49533904 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14-926G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49533904 | ||||||
chr10:49534064 | G | A | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-14-1086C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534064 | ||||||
chr10:49534133 | C | CA | 93 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0018others(90): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-14-1156dupT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534133 | ||||||
chr10:49534133 | C | CAA | 30 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0158others(27): Show | 32 | HG00609.hp1 HG00738.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.-14-1157_-14-1156d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534133 | ||||||
chr10:49534133 | CA | C | 74 | a0001c0004t0001g0247a0002c0002t0004g0007a0002c0002t0004g0008others(71): Show | 78 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-14-1156delT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534133 | ||||||
chr10:49534149 | A | AC | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-14-1172_-14-1171i others(3): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534149 | ||||||
chr10:49534149 | A | C | 1 | a0001c0005t0003g0257 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-14-1171T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534149 | ||||||
chr10:49534154 | A | C | 4 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237others(1): Show | 5 | HG02896.hp2 HG03209.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1176T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534154 | ||||||
chr10:49534155 | C | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0226a0002c0002t0004g0079others(2): Show | 7 | HG01952.hp1 HG01978.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1177G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534155 | ||||||
chr10:49534164 | A | C | 17 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0140others(14): Show | 20 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-1186T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534164 | ||||||
chr10:49534165 | A | AG | 2 | a0001c0001t0002g0004a0001c0001t0002g0226 | 4 | HG01952.hp1 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-1188_-14-1187i others(3): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534165 | ||||||
chr10:49534165 | A | G | 136 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0018others(133): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-14-1187T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534165 | ||||||
chr10:49534242 | C | T | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-14-1264G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534242 | ||||||
chr10:49534307 | T | C | 331 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(328): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.-14-1329A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534307 | ||||||
chr10:49534406 | G | A | 1 | a0001c0005t0025g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14-1428C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534406 | ||||||
chr10:49534407 | A | G | 315 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(312): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.-14-1429T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534407 | ||||||
chr10:49534417 | G | T | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-1439C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534417 | ||||||
chr10:49534432 | T | C | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0040t0002g0245 | 3 | HG00735.hp2 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-14-1454A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534432 | ||||||
chr10:49534565 | A | G | 40 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0013others(37): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-14-1587T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534565 | ||||||
chr10:49534605 | G | A | 53 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(50): Show | 63 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-14-1627C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534605 | ||||||
chr10:49534839 | C | CTTATTAA others(3): Show |
1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1871_-14-1862d others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534839 | ||||||
chr10:49534846 | A | G | 4 | a0001c0004t0007g0238a0001c0004t0007g0239a0001c0004t0007g0240others(1): Show | 4 | HG03017.hp1 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-1868T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534846 | ||||||
chr10:49534898 | C | G | 1 | a0003c0003t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-14-1920G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534898 | ||||||
chr10:49534961 | C | G | 2 | a0009c0013t0013g0034a0009c0013t0013g0329 | 3 | HG01243.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-1983G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49534961 | ||||||
chr10:49535038 | T | C | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-14-2060A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535038 | ||||||
chr10:49535042 | G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-14-2064C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535042 | ||||||
chr10:49535158 | T | C | 2 | a0016c0028t0001g0091a0018c0024t0001g0322 | 2 | HG01981.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2180A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535158 | ||||||
chr10:49535187 | G | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2209C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535187 | ||||||
chr10:49535279 | C | A | 3 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324 | 3 | HG02630.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-14-2301G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535279 | ||||||
chr10:49535320 | T | C | 1 | a0004c0006t0001g0319 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-14-2342A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535320 | ||||||
chr10:49535625 | C | T | 1 | a0002c0002t0006g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-2647G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535625 | ||||||
chr10:49535845 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-14-2867G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535845 | ||||||
chr10:49535850 | T | G | 1 | a0002c0002t0005g0080 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-14-2872A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49535850 | ||||||
chr10:49536107 | ACT | A | 31 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(28): Show | 39 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15+2853_-15+2854d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536107 | ||||||
chr10:49536117 | G | A | 1 | a0009c0013t0013g0329 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+2845C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536117 | ||||||
chr10:49536124 | T | C | 52 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(49): Show | 62 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-15+2838A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536124 | ||||||
chr10:49536144 | G | A | 1 | a0002c0002t0009g0204 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-15+2818C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536144 | ||||||
chr10:49536170 | G | A | 1 | a0023c0027t0001g0248 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+2792C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536170 | ||||||
chr10:49536214 | G | C | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-15+2748C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536214 | ||||||
chr10:49536260 | G | A | 52 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(49): Show | 62 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-15+2702C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536260 | ||||||
chr10:49536335 | C | A | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-15+2627G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536335 | ||||||
chr10:49536423 | A | G | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-15+2539T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536423 | ||||||
chr10:49536449 | G | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0227a0001c0001t0002g0229others(3): Show | 8 | HG00140.hp1 HG00280.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+2513C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536449 | ||||||
chr10:49536500 | G | A | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-15+2462C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536500 | ||||||
chr10:49536519 | T | A | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+2443A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536519 | ||||||
chr10:49536528 | A | C | 31 | a0002c0012t0014g0323a0002c0012t0014g0325a0002c0025t0014g0324others(28): Show | 39 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15+2434T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536528 | ||||||
chr10:49536691 | T | C | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+2271A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536691 | ||||||
chr10:49536692 | C | T | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+2270G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536692 | ||||||
chr10:49536856 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15+2106A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49536856 | ||||||
chr10:49537117 | G | A | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1845C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537117 | ||||||
chr10:49537217 | G | A | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-15+1745C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537217 | ||||||
chr10:49537236 | C | G | 1 | a0002c0012t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-15+1726G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537236 | ||||||
chr10:49537237 | G | A | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-15+1725C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537237 | ||||||
chr10:49537283 | G | A | 1 | a0005c0008t0001g0014 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+1679C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537283 | ||||||
chr10:49537342 | C | CA | 158 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(155): Show | 175 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-15+1619dupT | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537342 | ||||||
chr10:49537342 | C | CAA | 11 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237others(8): Show | 13 | HG00642.hp1 HG01243.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+1618_-15+1619d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537342 | ||||||
chr10:49537423 | T | C | 6 | a0006c0010t0008g0114a0006c0010t0008g0115a0006c0010t0008g0117others(3): Show | 6 | HG01069.hp2 HG01123.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1539A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537423 | ||||||
chr10:49537487 | C | CTA | 70 | a0001c0001t0002g0203a0001c0005t0003g0295a0002c0002t0004g0007others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-15+1473_-15+1474d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537487 | ||||||
chr10:49537487 | C | CTATA | 8 | a0002c0002t0004g0086a0002c0002t0004g0087a0002c0002t0005g0083others(5): Show | 8 | HG00438.hp2 HG01981.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+1471_-15+1474d others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537487 | ||||||
chr10:49537487 | CTATATA | C | 3 | a0001c0004t0011g0024a0001c0004t0011g0116a0001c0004t0011g0237 | 4 | HG02896.hp2 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+1469_-15+1474d others(8): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537487 | ||||||
chr10:49537488 | T | A | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+1474A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537488 | ||||||
chr10:49537501 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1461T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537501 | ||||||
chr10:49537502 | T | A | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1460A>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537502 | ||||||
chr10:49537502 | T | TAC | 3 | a0001c0004t0001g0143a0001c0004t0007g0249a0001c0004t0027g0250 | 3 | HG01106.hp1 HG02258.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-15+1458_-15+1459d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537502 | ||||||
chr10:49537502 | T | TACACAC | 4 | a0001c0004t0001g0016a0001c0004t0001g0144a0001c0004t0001g0145others(1): Show | 5 | HG02257.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+1459_-15+1460i others(8): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537502 | ||||||
chr10:49537502 | T | TACACACA others(1): Show |
7 | a0001c0004t0001g0146a0001c0004t0001g0147a0001c0004t0001g0148others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+1459_-15+1460i others(10): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537502 | ||||||
chr10:49537502 | T | TACACACA others(3): Show |
1 | a0001c0004t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-15+1459_-15+1460i others(12): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537502 | ||||||
chr10:49537505 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1457T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537505 | ||||||
chr10:49537508 | T | C | 14 | a0001c0004t0001g0016a0001c0004t0001g0140a0001c0004t0001g0143others(11): Show | 15 | HG01167.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+1454A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537508 | ||||||
chr10:49537508 | T | TAC | 44 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(41): Show | 50 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-15+1452_-15+1453d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537508 | ||||||
chr10:49537508 | T | TACAC | 37 | a0001c0001t0036g0233a0001c0004t0001g0122a0001c0004t0001g0123others(34): Show | 40 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-15+1450_-15+1453d others(6): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537508 | ||||||
chr10:49537508 | T | TACACAC | 10 | a0003c0003t0001g0013a0003c0003t0001g0106a0003c0003t0001g0107others(7): Show | 12 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+1448_-15+1453d others(8): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537508 | ||||||
chr10:49537508 | T | TACACACA others(1): Show |
2 | a0001c0004t0001g0015a0003c0003t0001g0112 | 3 | HG01433.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-15+1446_-15+1453d others(10): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537508 | ||||||
chr10:49537508 | TAC | T | 34 | a0001c0001t0002g0160a0001c0005t0003g0256a0001c0009t0002g0320others(31): Show | 42 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.-15+1452_-15+1453d others(4): Show |
ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537508 | ||||||
chr10:49537511 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1451T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537511 | ||||||
chr10:49537521 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1441T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537521 | ||||||
chr10:49537529 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1433T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537529 | ||||||
chr10:49537607 | A | G | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1355T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537607 | ||||||
chr10:49537617 | G | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1345C>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537617 | ||||||
chr10:49537649 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1313T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537649 | ||||||
chr10:49537659 | C | A | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1303G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537659 | ||||||
chr10:49537683 | T | G | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1279A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537683 | ||||||
chr10:49537684 | A | T | 1 | a0001c0009t0002g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+1278T>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537684 | ||||||
chr10:49537765 | G | A | 1 | a0006c0010t0008g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+1197C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537765 | ||||||
chr10:49537814 | C | A | 2 | a0014c0016t0018g0035a0021c0026t0030g0330 | 3 | HG02809.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-15+1148G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537814 | ||||||
chr10:49537815 | C | T | 1 | a0001c0004t0001g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15+1147G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537815 | ||||||
chr10:49537821 | C | G | 1 | a0007c0011t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+1141G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49537821 | ||||||
chr10:49538091 | G | A | 1 | a0007c0011t0001g0255 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+871C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538091 | ||||||
chr10:49538159 | C | G | 21 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0094others(18): Show | 23 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+803G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538159 | ||||||
chr10:49538178 | C | A | 2 | a0001c0005t0003g0298a0001c0005t0003g0299 | 2 | HG01978.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+784G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538178 | ||||||
chr10:49538192 | G | C | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-15+770C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538192 | ||||||
chr10:49538193 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-15+769G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538193 | ||||||
chr10:49538194 | T | C | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-15+768A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538194 | ||||||
chr10:49538255 | T | C | 55 | a0001c0005t0003g0003a0001c0005t0003g0027a0001c0005t0003g0029others(52): Show | 65 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-15+707A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538255 | ||||||
chr10:49538264 | A | C | 1 | a0001c0001t0002g0158 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-15+698T>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538264 | ||||||
chr10:49538329 | T | C | 1 | a0014c0016t0018g0035 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-15+633A>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538329 | ||||||
chr10:49538396 | T | G | 1 | a0001c0004t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-15+566A>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538396 | ||||||
chr10:49538730 | C | G | 11 | a0002c0002t0006g0333a0002c0002t0006g0334a0002c0002t0006g0336others(8): Show | 11 | HG00621.hp2 HG01891.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+232G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538730 | ||||||
chr10:49538806 | G | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-15+156C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538806 | ||||||
chr10:49538810 | A | G | 265 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(262): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-15+152T>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538810 | ||||||
chr10:49538817 | C | T | 1 | a0029c0036t0016g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-15+145G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538817 | ||||||
chr10:49538836 | C | T | 1 | a0001c0005t0026g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-15+126G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538836 | ||||||
chr10:49538875 | G | A | 1 | a0001c0004t0001g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+87C>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538875 | ||||||
chr10:49538877 | C | A | 106 | a0001c0009t0002g0320a0002c0002t0004g0007a0002c0002t0004g0008others(103): Show | 117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-15+85G>T | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538877 | ||||||
chr10:49538889 | GC | G | 342 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(339): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-15+72delG | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538889 | ||||||
chr10:49538892 | C | G | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+70G>C | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538892 | ||||||
chr10:49538893 | G | C | 1 | a0001c0005t0003g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+69C>G | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538893 | ||||||
chr10:49538938 | C | T | 1 | a0016c0028t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-15+24G>A | ERCC6 | ENSG00000225830.16 | transcript | ENST00000355832.10 | protein_coding | 1/20 | chr10 | 49538938 |