geneid | 1161 |
---|---|
ensemblid | ENSG00000049167.16 |
hgncid | 3439 |
symbol | ERCC8 |
name | ERCC excision repair 8, CSA ubiquitin ligase complex subunit |
refseq_nuc | NM_000082.4 |
refseq_prot | NP_000073.1 |
ensembl_nuc | ENST00000676185.1 |
ensembl_prot | ENSP00000501614.1 |
mane_status | MANE Select |
chr | chr5 |
start | 60866454 |
end | 60945070 |
strand | - |
ver | v1.2 |
region | chr5:60866454-60945070 |
region5000 | chr5:60861454-60950070 |
regionname0 | ERCC8_chr5_60866454_60945070 |
regionname5000 | ERCC8_chr5_60861454_60950070 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 396 | 301 | 88 | 56 | 104 | 16 | 35 | 82 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0002 | 0/0 | 396 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1191 | 249 | 77 | 37 | 97 | 10 | 26 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0002 | 0/0 | 1191 | 36 | 9 | 15 | 0 | 4 | 8 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0003 | 0/0 | 1191 | 6 | 0 | 3 | 0 | 2 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0004 | 0/0 | 1191 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0005 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0006 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0007 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0008 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
c0009 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8225 | 41 | 4 | 7 | 24 | 3 | 3 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0002 | 1/0 | 8224 | 34 | 0 | 8 | 17 | 1 | 7 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0003 | 0/0 | 8224 | 21 | 0 | 6 | 13 | 2 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0004 | 0/0 | 8221 | 14 | 0 | 2 | 12 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0005 | 0/1 | 8226 | 11 | 9 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0006 | 0/0 | 8225 | 10 | 1 | 4 | 0 | 0 | 5 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0007 | 0/0 | 8222 | 10 | 10 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0008 | 0/0 | 8210 | 9 | 1 | 4 | 0 | 3 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0009 | 0/0 | 8225 | 9 | 0 | 3 | 3 | 0 | 3 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0010 | 0/0 | 8223 | 9 | 9 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0011 | 0/0 | 8225 | 7 | 0 | 0 | 6 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0012 | 0/0 | 8225 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0013 | 0/0 | 8226 | 5 | 0 | 3 | 1 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0014 | 0/0 | 8224 | 5 | 5 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0015 | 0/0 | 8228 | 4 | 2 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0016 | 0/0 | 8210 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0017 | 0/0 | 8210 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0018 | 0/0 | 8227 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0019 | 0/0 | 8224 | 3 | 0 | 1 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0020 | 0/0 | 8224 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0021 | 0/0 | 8224 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0022 | 0/0 | 8221 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0023 | 0/0 | 8222 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0024 | 0/0 | 8221 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0025 | 0/0 | 8231 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0026 | 0/0 | 8232 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0027 | 0/0 | 8226 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0028 | 0/0 | 8228 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0029 | 0/0 | 8226 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0030 | 0/0 | 8224 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0031 | 0/0 | 8222 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0032 | 0/0 | 8211 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0033 | 0/0 | 8210 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0034 | 0/0 | 8226 | 2 | 1 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0035 | 0/0 | 8227 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0036 | 0/0 | 8227 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0037 | 0/0 | 8224 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0038 | 0/0 | 8225 | 2 | 0 | 0 | 1 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0039 | 0/0 | 8225 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0040 | 0/0 | 8225 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0041 | 0/0 | 8226 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0042 | 0/0 | 8224 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0043 | 0/0 | 8224 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0044 | 0/0 | 8211 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0045 | 0/0 | 8225 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0046 | 0/0 | 8226 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0047 | 0/0 | 8227 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0048 | 0/0 | 8227 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0049 | 0/0 | 8226 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0050 | 0/0 | 8226 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0051 | 0/0 | 8228 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0052 | 0/0 | 8224 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0053 | 0/0 | 8225 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0054 | 0/0 | 8226 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0055 | 0/0 | 8210 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0056 | 0/0 | 8210 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0057 | 0/0 | 8225 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0058 | 0/0 | 8227 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0059 | 0/0 | 8228 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0060 | 0/0 | 8227 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0061 | 0/0 | 8224 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0062 | 0/0 | 8225 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0063 | 0/0 | 8225 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0064 | 0/0 | 8225 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0065 | 0/0 | 8225 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0066 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0067 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0068 | 0/0 | 8228 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0069 | 0/0 | 8225 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0070 | 0/0 | 8225 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0071 | 0/0 | 8224 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0072 | 0/0 | 8224 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0073 | 0/0 | 8224 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0074 | 0/0 | 8225 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0075 | 0/0 | 8225 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0076 | 0/0 | 8201 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0077 | 0/0 | 8225 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0078 | 0/0 | 8225 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0079 | 0/0 | 8224 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0080 | 0/0 | 8224 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0081 | 0/0 | 8224 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0082 | 0/0 | 8219 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0083 | 0/0 | 8223 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0084 | 0/0 | 8221 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
t0085 | 0/0 | 8226 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1191 | 249 | 77 | 37 | 97 | 10 | 26 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002 | 0/0 | 1191 | 36 | 9 | 15 | 0 | 4 | 8 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0003 | 0/0 | 1191 | 6 | 0 | 3 | 0 | 2 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0004 | 0/0 | 1191 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0005 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0006 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0007 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0009 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0002c0008 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9415 | 38 | 4 | 7 | 21 | 3 | 3 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0002 | 1/0 | 9414 | 34 | 0 | 8 | 17 | 1 | 7 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0003 | 0/0 | 9414 | 20 | 0 | 6 | 12 | 2 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0004 | 0/0 | 9411 | 14 | 0 | 2 | 12 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0005 | 0/1 | 9416 | 11 | 9 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0007 | 0/0 | 9412 | 10 | 10 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0009 | 0/0 | 9415 | 9 | 0 | 3 | 3 | 0 | 3 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0010 | 0/0 | 9413 | 9 | 9 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0011 | 0/0 | 9415 | 7 | 0 | 0 | 6 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0012 | 0/0 | 9415 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0013 | 0/0 | 9416 | 4 | 0 | 2 | 1 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0014 | 0/0 | 9414 | 5 | 5 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0015 | 0/0 | 9418 | 4 | 2 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0018 | 0/0 | 9417 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0019 | 0/0 | 9414 | 3 | 0 | 1 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0020 | 0/0 | 9414 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0021 | 0/0 | 9414 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0022 | 0/0 | 9411 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0023 | 0/0 | 9412 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0027 | 0/0 | 9416 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0028 | 0/0 | 9418 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0029 | 0/0 | 9416 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0030 | 0/0 | 9414 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0031 | 0/0 | 9412 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0034 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0035 | 0/0 | 9417 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0036 | 0/0 | 9417 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0037 | 0/0 | 9414 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0038 | 0/0 | 9415 | 2 | 0 | 0 | 1 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0039 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0040 | 0/0 | 9415 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0041 | 0/0 | 9416 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0042 | 0/0 | 9414 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0043 | 0/0 | 9414 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0044 | 0/0 | 9401 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0045 | 0/0 | 9415 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0046 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0047 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0048 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0049 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0050 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0051 | 0/0 | 9418 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0058 | 0/0 | 9417 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0059 | 0/0 | 9418 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0060 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0061 | 0/0 | 9414 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0062 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0063 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0064 | 0/0 | 9415 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0065 | 0/0 | 9415 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0066 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0067 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0068 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0069 | 0/0 | 9415 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0070 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0071 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0072 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0073 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0074 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0075 | 0/0 | 9415 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0076 | 0/0 | 9391 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0077 | 0/0 | 9415 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0079 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0080 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0081 | 0/0 | 9414 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0082 | 0/0 | 9409 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0083 | 0/0 | 9413 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0084 | 0/0 | 9411 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0001t0085 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0006 | 0/0 | 9415 | 10 | 1 | 4 | 0 | 0 | 5 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0008 | 0/0 | 9400 | 8 | 1 | 4 | 0 | 3 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0016 | 0/0 | 9400 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0017 | 0/0 | 9400 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0032 | 0/0 | 9401 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0033 | 0/0 | 9400 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0052 | 0/0 | 9414 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0053 | 0/0 | 9415 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0054 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0055 | 0/0 | 9400 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0056 | 0/0 | 9400 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0002t0057 | 0/0 | 9415 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0003t0024 | 0/0 | 9411 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0003t0025 | 0/0 | 9421 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0003t0026 | 0/0 | 9422 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0004t0001 | 0/0 | 9415 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0004t0039 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0004t0078 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0005t0020 | 0/0 | 9414 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0006t0003 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0007t0013 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0001c0009t0034 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
a0002c0008t0008 | 0/0 | 9400 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | copy fasta | chr5 | 60861454 | 60950070 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0009g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0011g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0013g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0013g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0013g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0014g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0014g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0015g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0015g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0018g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0018g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0019g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0019g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0019g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0020g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0021g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0021g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0021g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0022g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0022g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0022g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0023g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0023g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0023g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0027g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0027g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0028g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0028g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0029g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0029g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0030g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0030g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0031g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0031g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0034g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0035g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0035g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0036g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0036g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0037g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0037g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0038g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0038g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0039g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0040g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0040g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0041g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0041g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0042g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0042g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0043g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0044g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0045g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0046g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0047g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0048g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0049g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0050g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0051g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0058g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0059g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0060g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0061g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0062g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0063g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0064g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0065g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0066g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0067g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0068g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0069g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0070g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0071g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0072g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0073g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0074g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0075g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0076g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0077g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0079g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0080g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0081g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0082g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0083g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0084g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0001t0085g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0016g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0016g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0016g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0017g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0017g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0017g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0017g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0032g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0032g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0033g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0033g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0052g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0053g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0054g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0055g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0056g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0002t0057g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0003t0024g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0003t0024g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0003t0025g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0003t0025g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0003t0026g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0003t0026g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0004t0039g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0004t0078g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0005t0020g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0006t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0007t0013g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0001c0009t0034g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
a0002c0008t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0050 | g0281 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00140 | hp1 | a0001 | c0002 | t0008 | g0080 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0200 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00280 | hp1 | a0001 | c0002 | t0057 | g0062 | EUR | FIN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0175 | EUR | FIN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00558 | hp2 | a0001 | c0001 | t0068 | g0133 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00621 | hp1 | a0001 | c0001 | t0067 | g0113 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00642 | hp1 | a0001 | c0002 | t0006 | g0058 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00642 | hp2 | a0001 | c0002 | t0033 | g0071 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00673 | hp1 | a0001 | c0001 | t0062 | g0101 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00733 | hp1 | a0001 | c0001 | t0009 | g0189 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00733 | hp2 | a0001 | c0007 | t0013 | g0129 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00735 | hp1 | a0001 | c0001 | t0009 | g0190 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00738 | hp1 | a0001 | c0002 | t0008 | g0073 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01069 | hp1 | a0001 | c0002 | t0008 | g0079 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01069 | hp2 | a0001 | c0001 | t0019 | g0159 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01099 | hp1 | a0001 | c0002 | t0017 | g0045 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0259 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01109 | hp2 | a0001 | c0003 | t0024 | g0008 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01167 | hp1 | a0001 | c0001 | t0018 | g0270 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01168 | hp1 | a0001 | c0001 | t0069 | g0138 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01168 | hp2 | a0001 | c0002 | t0017 | g0078 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01175 | hp1 | a0001 | c0001 | t0059 | g0263 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01175 | hp2 | a0001 | c0002 | t0017 | g0072 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01192 | hp1 | a0001 | c0002 | t0053 | g0055 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01192 | hp2 | a0001 | c0001 | t0043 | g0013 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01255 | hp2 | a0001 | c0002 | t0006 | g0057 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01257 | hp2 | a0001 | c0003 | t0025 | g0009 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01258 | hp2 | a0001 | c0003 | t0026 | g0010 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01346 | hp1 | a0001 | c0002 | t0017 | g0074 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01358 | hp2 | a0001 | c0002 | t0055 | g0081 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01361 | hp1 | a0001 | c0001 | t0042 | g0037 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01361 | hp2 | a0001 | c0001 | t0013 | g0148 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01433 | hp2 | a0001 | c0002 | t0008 | g0075 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01496 | hp2 | a0001 | c0002 | t0006 | g0061 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01515 | hp1 | a0001 | c0001 | t0038 | g0163 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01515 | hp2 | a0001 | c0003 | t0025 | g0012 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01516 | hp1 | a0001 | c0002 | t0008 | g0068 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01516 | hp2 | a0001 | c0001 | t0030 | g0253 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01517 | hp1 | a0001 | c0003 | t0026 | g0011 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01517 | hp2 | a0001 | c0001 | t0030 | g0254 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0033 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0293 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01928 | hp2 | a0001 | c0001 | t0035 | g0127 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01952 | hp2 | a0001 | c0002 | t0008 | g0065 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01981 | hp1 | a0001 | c0002 | t0006 | g0060 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0149 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02056 | hp1 | a0001 | c0001 | t0074 | g0052 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02056 | hp2 | a0001 | c0001 | t0073 | g0165 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02071 | hp1 | a0001 | c0004 | t0001 | g0160 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0157 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02080 | hp2 | a0001 | c0001 | t0070 | g0122 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02132 | hp1 | a0001 | c0001 | t0011 | g0111 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02132 | hp2 | a0001 | c0001 | t0031 | g0239 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02135 | hp2 | a0001 | c0001 | t0041 | g0232 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02145 | hp1 | a0001 | c0001 | t0018 | g0247 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02145 | hp2 | a0001 | c0002 | t0016 | g0070 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02257 | hp1 | a0001 | c0002 | t0056 | g0077 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02257 | hp2 | a0001 | c0001 | t0082 | g0014 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02258 | hp1 | a0001 | c0001 | t0027 | g0257 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02273 | hp2 | a0001 | c0001 | t0013 | g0126 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02280 | hp1 | a0001 | c0001 | t0046 | g0277 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0291 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02300 | hp2 | a0001 | c0001 | t0065 | g0144 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02451 | hp1 | a0001 | c0001 | t0014 | g0090 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02523 | hp2 | a0001 | c0001 | t0038 | g0103 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02572 | hp2 | a0001 | c0001 | t0044 | g0179 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02602 | hp1 | a0001 | c0001 | t0081 | g0220 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0275 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02615 | hp1 | a0001 | c0001 | t0037 | g0192 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02615 | hp2 | a0001 | c0001 | t0076 | g0054 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02622 | hp1 | a0001 | c0001 | t0083 | g0027 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0181 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02630 | hp2 | a0001 | c0001 | t0028 | g0039 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02647 | hp1 | a0001 | c0005 | t0020 | g0004 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02647 | hp2 | a0001 | c0001 | t0085 | g0180 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0207 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02683 | hp2 | a0001 | c0002 | t0033 | g0048 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02717 | hp1 | a0001 | c0001 | t0027 | g0256 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02717 | hp2 | a0001 | c0005 | t0020 | g0004 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0028 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02723 | hp2 | a0001 | c0001 | t0029 | g0265 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02735 | hp2 | a0001 | c0001 | t0058 | g0262 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02809 | hp1 | a0001 | c0001 | t0022 | g0290 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02809 | hp2 | a0001 | c0002 | t0016 | g0082 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0184 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0185 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02895 | hp2 | a0001 | c0002 | t0016 | g0064 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02896 | hp1 | a0001 | c0002 | t0016 | g0069 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0186 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0236 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02970 | hp1 | a0001 | c0001 | t0037 | g0191 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02970 | hp2 | a0001 | c0001 | t0015 | g0261 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03017 | hp1 | a0001 | c0003 | t0024 | g0007 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0260 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03098 | hp2 | a0001 | c0001 | t0084 | g0287 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03130 | hp1 | a0001 | c0001 | t0014 | g0091 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03130 | hp2 | a0001 | c0001 | t0018 | g0066 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03139 | hp1 | a0001 | c0001 | t0075 | g0095 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03139 | hp2 | a0001 | c0001 | t0022 | g0286 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03225 | hp1 | a0001 | c0001 | t0022 | g0288 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03486 | hp1 | a0001 | c0001 | t0060 | g0019 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0284 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03490 | hp1 | a0001 | c0002 | t0006 | g0084 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03516 | hp1 | a0001 | c0001 | t0034 | g0051 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0088 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03540 | hp1 | a0001 | c0002 | t0032 | g0063 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03540 | hp2 | a0001 | c0001 | t0014 | g0092 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03579 | hp1 | a0001 | c0001 | t0048 | g0279 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03579 | hp2 | a0001 | c0001 | t0023 | g0289 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03654 | hp1 | a0001 | c0001 | t0061 | g0096 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03704 | hp1 | a0001 | c0001 | t0011 | g0110 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03704 | hp2 | a0001 | c0002 | t0006 | g0083 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03710 | hp1 | a0001 | c0001 | t0045 | g0252 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0188 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03831 | hp1 | a0001 | c0002 | t0006 | g0059 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0292 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03927 | hp1 | a0001 | c0001 | t0041 | g0206 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03927 | hp2 | a0001 | c0002 | t0006 | g0178 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03942 | hp1 | a0001 | c0001 | t0015 | g0282 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03942 | hp2 | a0001 | c0001 | t0036 | g0154 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04115 | hp1 | a0001 | c0001 | t0051 | g0269 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04115 | hp2 | a0002 | c0008 | t0008 | g0076 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04184 | hp1 | a0001 | c0002 | t0054 | g0044 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04184 | hp2 | a0001 | c0001 | t0036 | g0156 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04199 | hp1 | a0001 | c0001 | t0013 | g0137 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04199 | hp2 | a0001 | c0002 | t0006 | g0049 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04204 | hp2 | a0001 | c0001 | t0064 | g0130 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04228 | hp1 | a0001 | c0002 | t0052 | g0022 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | CHB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18906 | hp1 | a0001 | c0001 | t0023 | g0285 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18940 | hp2 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18945 | hp2 | a0001 | c0001 | t0079 | g0218 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18953 | hp1 | a0001 | c0001 | t0019 | g0134 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18953 | hp2 | a0001 | c0001 | t0040 | g0227 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18957 | hp1 | a0001 | c0001 | t0021 | g0221 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18959 | hp2 | a0001 | c0004 | t0001 | g0100 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18962 | hp1 | a0001 | c0001 | t0080 | g0196 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18964 | hp2 | a0001 | c0001 | t0011 | g0173 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18970 | hp2 | a0001 | c0001 | t0063 | g0136 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18975 | hp1 | a0001 | c0001 | t0021 | g0201 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18975 | hp2 | a0001 | c0001 | t0066 | g0102 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18981 | hp2 | a0001 | c0001 | t0011 | g0167 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA18988 | hp2 | a0001 | c0001 | t0013 | g0153 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19003 | hp1 | a0001 | c0001 | t0072 | g0097 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19004 | hp1 | a0001 | c0001 | t0011 | g0093 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19004 | hp2 | a0001 | c0004 | t0078 | g0187 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19030 | hp2 | a0001 | c0001 | t0077 | g0021 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0183 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19056 | hp2 | a0001 | c0001 | t0071 | g0174 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19058 | hp1 | a0001 | c0006 | t0003 | g0087 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19060 | hp2 | a0001 | c0004 | t0001 | g0143 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19076 | hp1 | a0001 | c0001 | t0009 | g0229 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19076 | hp2 | a0001 | c0001 | t0039 | g0123 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19078 | hp1 | a0001 | c0001 | t0021 | g0224 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19081 | hp2 | a0001 | c0001 | t0035 | g0121 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19082 | hp1 | a0001 | c0001 | t0019 | g0132 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19082 | hp2 | a0001 | c0009 | t0034 | g0020 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19083 | hp2 | a0001 | c0001 | t0031 | g0242 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19084 | hp1 | a0001 | c0001 | t0040 | g0225 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19085 | hp1 | a0001 | c0001 | t0009 | g0223 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19086 | hp1 | a0001 | c0004 | t0039 | g0161 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ASW | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20129 | hp2 | a0001 | c0002 | t0006 | g0056 | AFR | ASW | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0164 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20805 | hp1 | a0001 | c0002 | t0008 | g0047 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | GIH | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02486 | hp1 | a0001 | c0001 | t0029 | g0264 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0089 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0030 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG02559 | hp2 | a0001 | c0002 | t0032 | g0067 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03471 | hp1 | a0001 | c0001 | t0028 | g0038 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG03471 | hp2 | a0001 | c0001 | t0049 | g0274 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
HG06807 | hp2 | a0001 | c0001 | t0047 | g0258 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20300 | hp1 | a0001 | c0002 | t0008 | g0046 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0108 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
NA21309 | hp2 | a0001 | c0001 | t0042 | g0023 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0248 | REF | REF | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0276 | REF | REF | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60904864
|
C | A | 1 | a0002 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.409G>T | p.Val137Leu | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/12 | 471/9414 | 409/1191 | 137/396 | chr5 | 60904864 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60887482
|
A | G | 1 | a0001c0004 | 5 | HG02071.hp1 NA18959.hp2 NA19004.hp2 others(2): Show |
synonymous_variant | LOW | c.1080T>C | p.Ala360Ala | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/12 | 1142/9414 | 1080/1191 | 360/396 | chr5 | 60887482 | ||
chr5:60891081
|
G | A | 1 | a0001c0007 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.849C>T | p.Asn283Asn | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/12 | 911/9414 | 849/1191 | 283/396 | chr5 | 60891081 | ||
chr5:60902507
|
A | T | 1 | a0001c0006 | 1 | NA19058.hp1 | splice_region_variant&synonymous_variant | LOW | c.552T>A | p.Gly184Gly | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/12 | 614/9414 | 552/1191 | 184/396 | chr5 | 60902507 | ||
chr5:60903694
|
T | C | 1 | a0001c0005 | 2 | HG02647.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.504A>G | p.Val168Val | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/12 | 566/9414 | 504/1191 | 168/396 | chr5 | 60903694 | ||
chr5:60904838
|
A | G | 2 | a0001c0002a0002c0008 | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
synonymous_variant | LOW | c.435T>C | p.Tyr145Tyr | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/12 | 497/9414 | 435/1191 | 145/396 | chr5 | 60904838 | ||
chr5:60918301
|
A | G | 1 | a0001c0003 | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
synonymous_variant | LOW | c.363T>C | p.Asp121Asp | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/12 | 425/9414 | 363/1191 | 121/396 | chr5 | 60918301 | ||
chr5:60922137
|
T | C | 1 | a0001c0009 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.192A>G | p.Ser64Ser | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/12 | 254/9414 | 192/1191 | 64/396 | chr5 | 60922137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60866519
|
C | T | 1 | a0001c0001t0071 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8096G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 8096 | chr5 | 60866519 | |||||
chr5:60866845
|
C | T | 1 | a0001c0002t0053 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7770G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7770 | chr5 | 60866845 | |||||
chr5:60866856
|
T | G | 13 | a0001c0002t0006a0001c0002t0008a0001c0002t0016others(10): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*7759A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7759 | chr5 | 60866856 | |||||
chr5:60866903
|
G | C | 1 | a0001c0001t0067 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7712C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7712 | chr5 | 60866903 | |||||
chr5:60866945
|
C | T | 1 | a0001c0001t0083 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7670G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7670 | chr5 | 60866945 | |||||
chr5:60867080
|
T | C | 84 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(81): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*7535A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7535 | chr5 | 60867080 | |||||
chr5:60867656
|
T | C | 4 | a0001c0001t0043a0001c0003t0024a0001c0003t0025others(1): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6959A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6959 | chr5 | 60867656 | |||||
chr5:60867689
|
T | G | 1 | a0001c0001t0065 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6926A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6926 | chr5 | 60867689 | |||||
chr5:60867768
|
CAGA | C | 3 | a0001c0003t0024a0001c0003t0025a0001c0003t0026 | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6844_*6846delTCT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6844 | chr5 | 60867768 | |||||
chr5:60867843
|
C | G | 84 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(81): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*6772G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6772 | chr5 | 60867843 | |||||
chr5:60867844
|
T | C | 1 | a0001c0001t0047 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6771A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6771 | chr5 | 60867844 | |||||
chr5:60867903
|
G | A | 1 | a0001c0001t0049 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6712C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6712 | chr5 | 60867903 | |||||
chr5:60868018
|
T | G | 35 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(32): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*6597A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6597 | chr5 | 60868018 | |||||
chr5:60868120
|
C | T | 1 | a0001c0001t0066 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6495G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6495 | chr5 | 60868120 | |||||
chr5:60868141
|
T | C | 1 | a0001c0001t0084 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6474A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6474 | chr5 | 60868141 | |||||
chr5:60868452
|
T | G | 4 | a0001c0001t0007a0001c0001t0010a0001c0001t0082others(1): Show | 21 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6163A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6163 | chr5 | 60868452 | |||||
chr5:60868715
|
T | C | 1 | a0001c0001t0028 | 2 | HG02630.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5900A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5900 | chr5 | 60868715 | |||||
chr5:60868786
|
G | A | 1 | a0001c0002t0056 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5829 | chr5 | 60868786 | |||||
chr5:60868857
|
A | G | 1 | a0001c0001t0075 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5758T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5758 | chr5 | 60868857 | |||||
chr5:60868949
|
C | T | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(31): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*5666G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5666 | chr5 | 60868949 | |||||
chr5:60868998
|
T | G | 1 | a0001c0002t0017 | 4 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5617A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5617 | chr5 | 60868998 | |||||
chr5:60869147
|
G | A | 7 | a0001c0001t0007a0001c0001t0010a0001c0001t0022others(4): Show | 28 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5468C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5468 | chr5 | 60869147 | |||||
chr5:60869373
|
G | A | 35 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(32): Show | 114 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*5242C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5242 | chr5 | 60869373 | |||||
chr5:60869412
|
T | A | 2 | a0001c0001t0050a0001c0001t0051 | 2 | HG00099.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5203A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5203 | chr5 | 60869412 | |||||
chr5:60869439
|
C | T | 1 | a0001c0001t0064 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5176G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5176 | chr5 | 60869439 | |||||
chr5:60869494
|
T | A | 1 | a0001c0001t0072 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5121A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5121 | chr5 | 60869494 | |||||
chr5:60869555
|
T | C | 1 | a0001c0001t0043 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5060A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5060 | chr5 | 60869555 | |||||
chr5:60869623
|
C | A | 1 | a0001c0001t0073 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4992G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4992 | chr5 | 60869623 | |||||
chr5:60869744
|
T | C | 1 | a0001c0004t0078 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4871A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4871 | chr5 | 60869744 | |||||
chr5:60869819
|
AAAGTG | A | 7 | a0001c0001t0007a0001c0001t0010a0001c0001t0022others(4): Show | 28 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4791_*4795delCACT others(1): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4791 | chr5 | 60869819 | |||||
chr5:60869875
|
C | A | 2 | a0001c0001t0012a0001c0001t0085 | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4740G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4740 | chr5 | 60869875 | |||||
chr5:60869960
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4655G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4655 | chr5 | 60869960 | |||||
chr5:60870043
|
TTCAAGTG others(17): Show |
T | 1 | a0001c0001t0076 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4548_*4571delGAAA others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4548 | chr5 | 60870043 | |||||
chr5:60870091
|
TAACAA | T | 2 | a0001c0001t0004a0001c0001t0031 | 16 | HG00673.hp2 HG02004.hp1 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4519_*4523delTTGT others(1): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4519 | chr5 | 60870091 | |||||
chr5:60870134
|
G | T | 1 | a0001c0001t0074 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4481C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4481 | chr5 | 60870134 | |||||
chr5:60870298
|
A | G | 1 | a0001c0001t0046 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4317T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4317 | chr5 | 60870298 | |||||
chr5:60870355
|
G | A | 1 | a0001c0002t0033 | 2 | HG00642.hp2 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4260C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4260 | chr5 | 60870355 | |||||
chr5:60870360
|
C | G | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(26): Show | 101 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*4255G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4255 | chr5 | 60870360 | |||||
chr5:60870367
|
G | A | 1 | a0001c0001t0037 | 2 | HG02615.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4248C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4248 | chr5 | 60870367 | |||||
chr5:60870372
|
G | A | 6 | a0001c0001t0028a0001c0001t0043a0001c0001t0044others(3): Show | 10 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4243C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4243 | chr5 | 60870372 | |||||
chr5:60870381
|
C | T | 1 | a0001c0001t0060 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4234G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4234 | chr5 | 60870381 | |||||
chr5:60870482
|
T | TA | 22 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(19): Show | 90 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4132dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | |||||
chr5:60870482
|
T | TAA | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0013others(16): Show | 50 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*4131_*4132dupTT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | |||||
chr5:60870482
|
T | TAAA | 9 | a0001c0001t0007a0001c0001t0018a0001c0001t0023others(6): Show | 24 | HG01167.hp1 HG01891.hp1 HG01928.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4130_*4132dupTTT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | |||||
chr5:60870482
|
T | TAAAA | 6 | a0001c0001t0010a0001c0001t0015a0001c0001t0028others(3): Show | 18 | HG00558.hp2 HG01109.hp1 HG01175.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4129_*4132dupTTTT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | |||||
chr5:60870482
|
T | TAAAAAAA others(3): Show |
1 | a0001c0003t0025 | 2 | HG01257.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4123_*4132dupTTTT others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | |||||
chr5:60870482
|
T | TAAAAAAA others(4): Show |
1 | a0001c0003t0026 | 2 | HG01258.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4122_*4132dupTTTT others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | |||||
chr5:60870482
|
TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0044a0001c0002t0032 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4120_*4132delTTTT others(9): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4120 | chr5 | 60870482 | |||||
chr5:60870482
|
TAAAAAAA others(7): Show |
T | 7 | a0001c0002t0008a0001c0002t0016a0001c0002t0017others(4): Show | 21 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4119_*4132delTTTT others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4119 | chr5 | 60870482 | |||||
chr5:60870523
|
G | A | 7 | a0001c0001t0007a0001c0001t0010a0001c0001t0022others(4): Show | 28 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4092C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4092 | chr5 | 60870523 | |||||
chr5:60870618
|
C | T | 6 | a0001c0001t0034a0001c0001t0058a0001c0001t0059others(3): Show | 6 | HG01175.hp1 HG01358.hp2 HG02735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3997G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3997 | chr5 | 60870618 | |||||
chr5:60870619
|
G | A | 1 | a0001c0001t0069 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3996C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3996 | chr5 | 60870619 | |||||
chr5:60870946
|
T | A | 1 | a0001c0001t0043 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3669A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3669 | chr5 | 60870946 | |||||
chr5:60870972
|
G | GA | 7 | a0001c0001t0036a0001c0001t0038a0001c0001t0040others(4): Show | 11 | HG01515.hp1 HG02080.hp2 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3642dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3642 | chr5 | 60870972 | |||||
chr5:60870981
|
C | A | 6 | a0001c0002t0008a0001c0002t0017a0001c0002t0033others(3): Show | 17 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3634G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3634 | chr5 | 60870981 | |||||
chr5:60871082
|
C | T | 4 | a0001c0001t0043a0001c0003t0024a0001c0003t0025others(1): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3533G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3533 | chr5 | 60871082 | |||||
chr5:60871115
|
A | G | 1 | a0001c0001t0080 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3500T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3500 | chr5 | 60871115 | |||||
chr5:60871147
|
A | G | 1 | a0001c0001t0021 | 3 | NA18957.hp1 NA18975.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3468T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3468 | chr5 | 60871147 | |||||
chr5:60871193
|
A | C | 84 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(81): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*3422T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3422 | chr5 | 60871193 | |||||
chr5:60871380
|
C | T | 3 | a0001c0001t0022a0001c0001t0023a0001c0001t0084 | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3235G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3235 | chr5 | 60871380 | |||||
chr5:60871855
|
T | C | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2760A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2760 | chr5 | 60871855 | |||||
chr5:60871888
|
C | A | 1 | a0001c0001t0049 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2727 | chr5 | 60871888 | |||||
chr5:60872061
|
A | C | 19 | a0001c0001t0001a0001c0001t0013a0001c0001t0019others(16): Show | 65 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2554T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2554 | chr5 | 60872061 | |||||
chr5:60872084
|
G | A | 1 | a0001c0001t0014 | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2531C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2531 | chr5 | 60872084 | |||||
chr5:60872213
|
A | T | 1 | a0001c0001t0062 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2402T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2402 | chr5 | 60872213 | |||||
chr5:60872338
|
A | C | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*2277T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2277 | chr5 | 60872338 | |||||
chr5:60872382
|
G | T | 1 | a0001c0001t0079 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2233C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2233 | chr5 | 60872382 | |||||
chr5:60872756
|
G | A | 3 | a0001c0001t0039a0001c0004t0039a0001c0004t0078 | 3 | NA19004.hp2 NA19076.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1859C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1859 | chr5 | 60872756 | |||||
chr5:60872810
|
G | C | 5 | a0001c0001t0034a0001c0001t0058a0001c0001t0059others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1805C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1805 | chr5 | 60872810 | |||||
chr5:60872881
|
T | C | 2 | a0001c0001t0050a0001c0001t0051 | 2 | HG00099.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1734A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1734 | chr5 | 60872881 | |||||
chr5:60873068
|
G | A | 3 | a0001c0001t0034a0001c0001t0060a0001c0009t0034 | 3 | HG03486.hp1 HG03516.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1547C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1547 | chr5 | 60873068 | |||||
chr5:60873145
|
A | G | 13 | a0001c0002t0006a0001c0002t0008a0001c0002t0016others(10): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1470T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1470 | chr5 | 60873145 | |||||
chr5:60873210
|
T | C | 1 | a0001c0001t0081 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1405A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1405 | chr5 | 60873210 | |||||
chr5:60873273
|
T | C | 4 | a0001c0001t0043a0001c0003t0024a0001c0003t0025others(1): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1342A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1342 | chr5 | 60873273 | |||||
chr5:60873287
|
C | T | 84 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(81): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1328 | chr5 | 60873287 | |||||
chr5:60873324
|
T | C | 13 | a0001c0002t0006a0001c0002t0008a0001c0002t0016others(10): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1291A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1291 | chr5 | 60873324 | |||||
chr5:60873445
|
C | T | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1170G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1170 | chr5 | 60873445 | |||||
chr5:60873472
|
C | T | 4 | a0001c0001t0043a0001c0003t0024a0001c0003t0025others(1): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1143G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1143 | chr5 | 60873472 | |||||
chr5:60873500
|
C | T | 1 | a0001c0001t0029 | 2 | HG02486.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1115G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1115 | chr5 | 60873500 | |||||
chr5:60873533
|
C | T | 6 | a0001c0001t0028a0001c0001t0043a0001c0001t0044others(3): Show | 10 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1082G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1082 | chr5 | 60873533 | |||||
chr5:60873578
|
T | G | 48 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(45): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1037A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1037 | chr5 | 60873578 | |||||
chr5:60873655
|
C | A | 7 | a0001c0001t0012a0001c0001t0034a0001c0001t0058others(4): Show | 12 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*960G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 960 | chr5 | 60873655 | |||||
chr5:60873831
|
G | A | 1 | a0001c0002t0057 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 784 | chr5 | 60873831 | |||||
chr5:60874032
|
A | G | 1 | a0001c0001t0027 | 2 | HG02258.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*583T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 583 | chr5 | 60874032 | |||||
chr5:60874096
|
G | T | 5 | a0001c0001t0007a0001c0001t0010a0001c0001t0042others(2): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*519C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 519 | chr5 | 60874096 | |||||
chr5:60874176
|
C | A | 10 | a0001c0001t0007a0001c0001t0010a0001c0001t0012others(7): Show | 37 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*439G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 439 | chr5 | 60874176 | |||||
chr5:60874378
|
A | G | 5 | a0001c0001t0034a0001c0001t0058a0001c0001t0059others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*237T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 237 | chr5 | 60874378 | |||||
chr5:60874510
|
A | G | 34 | a0001c0001t0004a0001c0001t0005a0001c0001t0015others(31): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 105 | chr5 | 60874510 | |||||
chr5:60874579
|
G | A | 1 | a0001c0001t0014 | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 36 | chr5 | 60874579 | |||||
chr5:60945031
|
A | C | 4 | a0001c0001t0043a0001c0003t0024a0001c0003t0025others(1): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/12 | 23 | chr5 | 60945031 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60874731
|
T | C | 46 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(43): Show | 47 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1123-48A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60874731 | ||||||
chr5:60874778
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(104): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1123-95A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60874778 | ||||||
chr5:60875007
|
G | C | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1123-324C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875007 | ||||||
chr5:60875015
|
T | C | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0009g0189others(1): Show | 4 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1123-332A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875015 | ||||||
chr5:60875150
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-467G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875150 | ||||||
chr5:60875243
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1123-560A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875243 | ||||||
chr5:60875340
|
C | G | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123-657G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875340 | ||||||
chr5:60875711
|
T | C | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1123-1028A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875711 | ||||||
chr5:60875855
|
C | T | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1123-1172G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875855 | ||||||
chr5:60875886
|
A | C | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123-1203T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875886 | ||||||
chr5:60875893
|
C | CT | 48 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(45): Show | 49 | HG01109.hp2 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1123-1211dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875893 | ||||||
chr5:60875893
|
C | CTT | 86 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1123-1212_1123-121 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875893 | ||||||
chr5:60875937
|
G | A | 1 | a0001c0001t0036g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1123-1254C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875937 | ||||||
chr5:60876029
|
T | C | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-1346A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876029 | ||||||
chr5:60876053
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1123-1370C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876053 | ||||||
chr5:60876080
|
G | C | 93 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1123-1397C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876080 | ||||||
chr5:60876083
|
G | A | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-1400C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876083 | ||||||
chr5:60876341
|
C | T | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-1658G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876341 | ||||||
chr5:60876369
|
T | A | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1123-1686A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876369 | ||||||
chr5:60876392
|
C | T | 1 | a0001c0001t0065g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1123-1709G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876392 | ||||||
chr5:60876547
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1864G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876547 | ||||||
chr5:60876558
|
T | C | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1875A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876558 | ||||||
chr5:60876565
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1882G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876565 | ||||||
chr5:60876566
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1883T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876566 | ||||||
chr5:60876572
|
C | G | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1889G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876572 | ||||||
chr5:60876583
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1900C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876583 | ||||||
chr5:60876692
|
T | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-2009A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876692 | ||||||
chr5:60876763
|
G | A | 1 | a0001c0001t0003g0050 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1123-2080C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876763 | ||||||
chr5:60876787
|
G | C | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-2104C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876787 | ||||||
chr5:60876819
|
A | T | 12 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(9): Show | 12 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1123-2136T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876819 | ||||||
chr5:60876884
|
A | G | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123-2201T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876884 | ||||||
chr5:60876913
|
T | G | 93 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1123-2230A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876913 | ||||||
chr5:60876990
|
C | A | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1123-2307G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876990 | ||||||
chr5:60877195
|
T | C | 2 | a0001c0001t0037g0191a0001c0001t0037g0192 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1123-2512A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877195 | ||||||
chr5:60877219
|
G | C | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-2536C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877219 | ||||||
chr5:60877230
|
T | A | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1123-2547A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877230 | ||||||
chr5:60877360
|
C | T | 1 | a0001c0001t0012g0182 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1123-2677G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877360 | ||||||
chr5:60877408
|
G | A | 1 | a0001c0001t0079g0218 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1123-2725C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877408 | ||||||
chr5:60877448
|
C | CATGGCAT others(5): Show |
1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2766_1123-276 others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877448 | ||||||
chr5:60877481
|
A | C | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2798T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877481 | ||||||
chr5:60877482
|
C | A | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2799G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877482 | ||||||
chr5:60877496
|
C | A | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2813G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877496 | ||||||
chr5:60877548
|
C | A | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2865G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877548 | ||||||
chr5:60877551
|
T | G | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2868A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877551 | ||||||
chr5:60877552
|
G | T | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2869C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877552 | ||||||
chr5:60877568
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1123-2885T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877568 | ||||||
chr5:60877576
|
G | A | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2893C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877576 | ||||||
chr5:60877577
|
A | G | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2894T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877577 | ||||||
chr5:60877580
|
A | C | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2897T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877580 | ||||||
chr5:60877585
|
C | T | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2902G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877585 | ||||||
chr5:60877588
|
C | A | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2905G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877588 | ||||||
chr5:60877623
|
A | G | 1 | a0001c0001t0009g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1123-2940T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877623 | ||||||
chr5:60877710
|
C | T | 1 | a0001c0001t0041g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1123-3027G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877710 | ||||||
chr5:60877758
|
A | G | 1 | a0001c0001t0019g0159 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1123-3075T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877758 | ||||||
chr5:60877784
|
G | T | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-3101C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877784 | ||||||
chr5:60877792
|
A | T | 10 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0043g0013others(7): Show | 10 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1123-3109T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877792 | ||||||
chr5:60877950
|
T | A | 1 | a0001c0001t0049g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1123-3267A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877950 | ||||||
chr5:60877967
|
C | G | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-3284G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877967 | ||||||
chr5:60878041
|
G | A | 6 | a0001c0003t0024g0007a0001c0003t0024g0008a0001c0003t0025g0009others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1123-3358C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878041 | ||||||
chr5:60878164
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0080g0196 | 3 | NA18939.hp2 NA18962.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1123-3481G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878164 | ||||||
chr5:60878230
|
C | A | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1123-3547G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878230 | ||||||
chr5:60878385
|
T | A | 3 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0043 | 3 | NA18963.hp1 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1123-3702A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878385 | ||||||
chr5:60878480
|
G | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1123-3797C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878480 | ||||||
chr5:60878486
|
C | G | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1123-3803G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878486 | ||||||
chr5:60878502
|
G | A | 1 | a0001c0001t0063g0136 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1123-3819C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878502 | ||||||
chr5:60878507
|
T | C | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1123-3824A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878507 | ||||||
chr5:60878572
|
A | T | 2 | a0001c0001t0058g0262a0001c0001t0059g0263 | 2 | HG01175.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1123-3889T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878572 | ||||||
chr5:60878595
|
C | G | 1 | a0001c0001t0029g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1123-3912G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878595 | ||||||
chr5:60878656
|
C | G | 6 | a0001c0003t0024g0007a0001c0003t0024g0008a0001c0003t0025g0009others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1123-3973G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878656 | ||||||
chr5:60878716
|
T | A | 4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1123-4033A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878716 | ||||||
chr5:60878733
|
T | TA | 37 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1123-4051_1123-405 others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878733 | ||||||
chr5:60878875
|
C | G | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1123-4192G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878875 | ||||||
chr5:60878904
|
C | T | 1 | a0001c0001t0031g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1123-4221G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878904 | ||||||
chr5:60878948
|
T | C | 37 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1123-4265A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878948 | ||||||
chr5:60879146
|
G | C | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1123-4463C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879146 | ||||||
chr5:60879168
|
G | T | 40 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(37): Show | 41 | HG00099.hp1 HG00673.hp2 HG01516.hp2 others(38): Show |
intron_variant | MODIFIER | c.1123-4485C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879168 | ||||||
chr5:60879174
|
C | T | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1123-4491G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879174 | ||||||
chr5:60879180
|
T | C | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1123-4497A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879180 | ||||||
chr5:60879203
|
T | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-4520A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879203 | ||||||
chr5:60879205
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(103): Show | 111 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1123-4522G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879205 | ||||||
chr5:60879549
|
G | C | 1 | a0001c0002t0016g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1123-4866C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879549 | ||||||
chr5:60879596
|
T | C | 1 | a0001c0004t0078g0187 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1123-4913A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879596 | ||||||
chr5:60879748
|
C | G | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-5065G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879748 | ||||||
chr5:60879896
|
G | C | 1 | a0001c0001t0072g0097 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1123-5213C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879896 | ||||||
chr5:60879907
|
G | T | 83 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1123-5224C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879907 | ||||||
chr5:60879919
|
T | C | 1 | a0001c0007t0013g0129 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1123-5236A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879919 | ||||||
chr5:60880002
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0267 | 3 | NA18968.hp1 NA18973.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1123-5319T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880002 | ||||||
chr5:60880194
|
C | A | 1 | a0001c0001t0031g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1123-5511G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880194 | ||||||
chr5:60880271
|
C | T | 1 | a0001c0001t0007g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1123-5588G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880271 | ||||||
chr5:60880297
|
C | T | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-5614G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880297 | ||||||
chr5:60880317
|
C | T | 1 | a0001c0001t0013g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1123-5634G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880317 | ||||||
chr5:60880372
|
T | C | 5 | a0001c0001t0007g0025a0001c0001t0010g0002a0001c0001t0010g0026others(2): Show | 6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123-5689A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880372 | ||||||
chr5:60880401
|
A | T | 1 | a0001c0004t0001g0143 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1123-5718T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880401 | ||||||
chr5:60880409
|
C | T | 83 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1123-5726G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880409 | ||||||
chr5:60880507
|
A | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(104): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1123-5824T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880507 | ||||||
chr5:60880536
|
C | T | 8 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0002g0202others(5): Show | 8 | HG03490.hp2 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123-5853G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880536 | ||||||
chr5:60880590
|
C | T | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1123-5907G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880590 | ||||||
chr5:60880674
|
A | G | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1123-5991T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880674 | ||||||
chr5:60880684
|
C | T | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1123-6001G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880684 | ||||||
chr5:60880721
|
C | A | 1 | a0001c0001t0002g0222 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1123-6038G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880721 | ||||||
chr5:60880721
|
C | T | 46 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(43): Show | 47 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1123-6038G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880721 | ||||||
chr5:60880725
|
A | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1123-6042T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880725 | ||||||
chr5:60880808
|
A | G | 1 | a0001c0001t0060g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1123-6125T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880808 | ||||||
chr5:60880841
|
G | A | 2 | a0001c0001t0001g0147a0001c0002t0052g0022 | 2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1123-6158C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880841 | ||||||
chr5:60880865
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-6182G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880865 | ||||||
chr5:60880940
|
C | G | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-6257G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880940 | ||||||
chr5:60880944
|
C | G | 13 | a0001c0001t0002g0005a0001c0001t0002g0219a0001c0001t0002g0222others(10): Show | 14 | NA18940.hp2 NA18942.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1123-6261G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880944 | ||||||
chr5:60880967
|
G | T | 6 | a0001c0001t0005g0271a0001c0001t0018g0066a0001c0001t0027g0256others(3): Show | 6 | HG00099.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123-6284C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880967 | ||||||
chr5:60880968
|
C | T | 6 | a0001c0001t0005g0271a0001c0001t0018g0066a0001c0001t0027g0256others(3): Show | 6 | HG00099.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123-6285G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880968 | ||||||
chr5:60881026
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1123-6343C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881026 | ||||||
chr5:60881150
|
ATCAG | A | 46 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(43): Show | 47 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1122+6286_1122+628 others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881150 | ||||||
chr5:60881162
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1122+6278T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881162 | ||||||
chr5:60881192
|
A | C | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1122+6248T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881192 | ||||||
chr5:60881263
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1122+6177G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881263 | ||||||
chr5:60881288
|
A | G | 2 | a0001c0001t0037g0191a0001c0001t0037g0192 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1122+6152T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881288 | ||||||
chr5:60881319
|
G | A | 5 | a0001c0001t0014g0088a0001c0001t0014g0089a0001c0001t0014g0090others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+6121C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881319 | ||||||
chr5:60881328
|
G | C | 5 | a0001c0001t0014g0088a0001c0001t0014g0089a0001c0001t0014g0090others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+6112C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881328 | ||||||
chr5:60881475
|
C | T | 46 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(43): Show | 47 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1122+5965G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881475 | ||||||
chr5:60881510
|
A | T | 1 | a0001c0005t0020g0004 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1122+5930T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881510 | ||||||
chr5:60881613
|
T | C | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+5827A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881613 | ||||||
chr5:60881624
|
T | C | 6 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122+5816A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881624 | ||||||
chr5:60881642
|
C | A | 1 | a0001c0001t0007g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1122+5798G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881642 | ||||||
chr5:60881643
|
G | A | 43 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(40): Show | 44 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.1122+5797C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881643 | ||||||
chr5:60881663
|
C | T | 1 | a0001c0003t0024g0007 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1122+5777G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881663 | ||||||
chr5:60881700
|
C | G | 14 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+5740G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881700 | ||||||
chr5:60881752
|
G | A | 2 | a0001c0001t0034g0051a0001c0001t0060g0019 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1122+5688C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881752 | ||||||
chr5:60881785
|
A | G | 1 | a0001c0001t0067g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1122+5655T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881785 | ||||||
chr5:60881794
|
C | T | 1 | a0001c0001t0022g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1122+5646G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881794 | ||||||
chr5:60881796
|
C | T | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+5644G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881796 | ||||||
chr5:60881851
|
C | A | 41 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(38): Show | 42 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1122+5589G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881851 | ||||||
chr5:60881852
|
G | A | 2 | a0001c0001t0005g0271a0001c0001t0018g0066 | 2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1122+5588C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881852 | ||||||
chr5:60881924
|
G | C | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1122+5516C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881924 | ||||||
chr5:60881954
|
C | T | 2 | a0001c0001t0004g0249a0001c0001t0004g0273 | 2 | HG00673.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1122+5486G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881954 | ||||||
chr5:60882010
|
T | G | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+5430A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882010 | ||||||
chr5:60882031
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1122+5409G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882031 | ||||||
chr5:60882043
|
G | A | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1122+5397C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882043 | ||||||
chr5:60882260
|
G | A | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1122+5180C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882260 | ||||||
chr5:60882268
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1122+5172T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882268 | ||||||
chr5:60882301
|
G | A | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1122+5139C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882301 | ||||||
chr5:60882309
|
T | A | 7 | a0001c0001t0001g0099a0001c0001t0039g0123a0001c0004t0001g0100others(4): Show | 7 | HG02071.hp1 NA18944.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+5131A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882309 | ||||||
chr5:60882348
|
A | T | 13 | a0001c0001t0002g0005a0001c0001t0002g0219a0001c0001t0002g0222others(10): Show | 14 | NA18940.hp2 NA18942.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+5092T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882348 | ||||||
chr5:60882462
|
T | C | 1 | a0001c0001t0022g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1122+4978A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882462 | ||||||
chr5:60882662
|
C | T | 2 | a0001c0002t0006g0059a0001c0002t0054g0044 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1122+4778G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882662 | ||||||
chr5:60882666
|
C | T | 5 | a0001c0001t0005g0278a0001c0001t0014g0089a0001c0001t0014g0090others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122+4774G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882666 | ||||||
chr5:60882671
|
G | C | 1 | a0001c0001t0002g0210 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1122+4769C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882671 | ||||||
chr5:60882834
|
A | C | 1 | a0001c0002t0006g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1122+4606T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882834 | ||||||
chr5:60882911
|
A | G | 1 | a0001c0001t0005g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1122+4529T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882911 | ||||||
chr5:60882970
|
A | AAC | 62 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0094others(59): Show | 63 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1122+4468_1122+446 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | ||||||
chr5:60882970
|
A | AACAC | 14 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0002g0200others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+4466_1122+446 others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | ||||||
chr5:60882970
|
A | AACACAC | 26 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(23): Show | 27 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1122+4464_1122+446 others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | ||||||
chr5:60882970
|
A | AACACACA others(1): Show |
9 | a0001c0001t0007g0032a0001c0001t0007g0035a0001c0001t0015g0260others(6): Show | 9 | HG02630.hp1 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+4462_1122+446 others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | ||||||
chr5:60882970
|
A | AACACACA others(3): Show |
1 | a0001c0001t0023g0284 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1122+4460_1122+446 others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | ||||||
chr5:60882970
|
AAC | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+4468_1122+446 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | ||||||
chr5:60883004
|
CAT | C | 3 | a0001c0001t0027g0256a0001c0001t0027g0257a0001c0001t0028g0039 | 3 | HG02258.hp1 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1122+4434_1122+443 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883004 | ||||||
chr5:60883006
|
T | C | 93 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1122+4434A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883006 | ||||||
chr5:60883007
|
G | A | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1122+4433C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883007 | ||||||
chr5:60883023
|
G | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+4417C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883023 | ||||||
chr5:60883132
|
T | A | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1122+4308A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883132 | ||||||
chr5:60883227
|
G | A | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1122+4213C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883227 | ||||||
chr5:60883319
|
G | A | 1 | a0001c0001t0009g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1122+4121C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883319 | ||||||
chr5:60883320
|
T | G | 1 | a0001c0001t0009g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1122+4120A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883320 | ||||||
chr5:60883321
|
A | T | 1 | a0001c0001t0009g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1122+4119T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883321 | ||||||
chr5:60883335
|
T | C | 1 | a0001c0001t0042g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1122+4105A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883335 | ||||||
chr5:60883468
|
T | C | 1 | a0001c0001t0023g0284 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1122+3972A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883468 | ||||||
chr5:60883474
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(247): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1122+3966T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883474 | ||||||
chr5:60883491
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1122+3949A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883491 | ||||||
chr5:60883533
|
C | A | 17 | a0001c0002t0008g0046a0001c0002t0008g0047a0001c0002t0008g0065others(14): Show | 17 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1122+3907G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883533 | ||||||
chr5:60883555
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1122+3885C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883555 | ||||||
chr5:60884111
|
T | C | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0118 | 3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1122+3329A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884111 | ||||||
chr5:60884173
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+3267G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884173 | ||||||
chr5:60884250
|
C | T | 4 | a0001c0001t0005g0250a0001c0001t0005g0251a0001c0001t0005g0255others(1): Show | 4 | HG02886.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+3190G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884250 | ||||||
chr5:60884252
|
G | A | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1122+3188C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884252 | ||||||
chr5:60884312
|
T | C | 1 | a0001c0003t0024g0008 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1122+3128A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884312 | ||||||
chr5:60884408
|
G | A | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122+3032C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884408 | ||||||
chr5:60884424
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1122+3016G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884424 | ||||||
chr5:60884448
|
C | A | 1 | a0001c0002t0016g0064 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1122+2992G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884448 | ||||||
chr5:60884475
|
C | CA | 12 | a0001c0001t0002g0036a0001c0001t0002g0212a0001c0001t0009g0205others(9): Show | 12 | HG00621.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1122+2964dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884475 | ||||||
chr5:60884475
|
CA | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(189): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1122+2964delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884475 | ||||||
chr5:60884487
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1122+2953T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884487 | ||||||
chr5:60884523
|
G | GT | 54 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(51): Show | 55 | HG00099.hp1 HG00673.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.1122+2916dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884523 | ||||||
chr5:60884523
|
G | GTTT | 31 | a0001c0002t0006g0056a0001c0002t0006g0057a0001c0002t0006g0058others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1122+2914_1122+291 others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884523 | ||||||
chr5:60884523
|
GT | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(99): Show | 107 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1122+2916delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884523 | ||||||
chr5:60884532
|
T | G | 1 | a0001c0001t0014g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1122+2908A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884532 | ||||||
chr5:60884647
|
C | T | 23 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(20): Show | 24 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1122+2793G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884647 | ||||||
chr5:60884786
|
T | C | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1122+2654A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884786 | ||||||
chr5:60885014
|
CT | C | 48 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(45): Show | 49 | HG01109.hp2 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1122+2425delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885014 | ||||||
chr5:60885039
|
A | ACAGGTGA others(4): Show |
4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+2400_1122+240 others(15): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885039 | ||||||
chr5:60885040
|
T | A | 4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+2400A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885040 | ||||||
chr5:60885107
|
G | C | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1122+2333C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885107 | ||||||
chr5:60885155
|
G | C | 6 | a0001c0003t0024g0007a0001c0003t0024g0008a0001c0003t0025g0009others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122+2285C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885155 | ||||||
chr5:60885221
|
G | A | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+2219C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885221 | ||||||
chr5:60885307
|
C | A | 93 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1122+2133G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885307 | ||||||
chr5:60885419
|
G | T | 1 | a0001c0001t0039g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1122+2021C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885419 | ||||||
chr5:60885613
|
T | C | 1 | a0001c0001t0003g0085 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1122+1827A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885613 | ||||||
chr5:60885673
|
T | C | 83 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1122+1767A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885673 | ||||||
chr5:60885779
|
T | C | 6 | a0001c0003t0024g0007a0001c0003t0024g0008a0001c0003t0025g0009others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122+1661A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885779 | ||||||
chr5:60885861
|
G | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+1579C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885861 | ||||||
chr5:60886066
|
G | GTA | 38 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(35): Show | 39 | HG00099.hp1 HG00673.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.1122+1372_1122+137 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886066 | ||||||
chr5:60886182
|
T | C | 1 | a0001c0002t0006g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1122+1258A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886182 | ||||||
chr5:60886395
|
G | A | 122 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1122+1045C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886395 | ||||||
chr5:60886470
|
G | C | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1122+970C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886470 | ||||||
chr5:60886497
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(117): Show | 125 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1122+943A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886497 | ||||||
chr5:60886571
|
G | A | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+869C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886571 | ||||||
chr5:60886573
|
G | A | 1 | a0001c0001t0031g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1122+867C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886573 | ||||||
chr5:60886651
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1122+789T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886651 | ||||||
chr5:60886687
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1122+753A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886687 | ||||||
chr5:60886703
|
A | AAAAAAT | 53 | a0001c0001t0002g0193a0001c0001t0002g0230a0001c0001t0004g0237others(50): Show | 54 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1122+731_1122+736d others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | ||||||
chr5:60886703
|
A | AAAAAATA others(5): Show |
26 | a0001c0001t0005g0248a0001c0001t0005g0268a0001c0001t0007g0015others(23): Show | 27 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1122+725_1122+736d others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | ||||||
chr5:60886703
|
AAAAAAT | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0241a0001c0001t0004g0243others(12): Show | 16 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1122+731_1122+736d others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | ||||||
chr5:60886703
|
AAAAAATA others(5): Show |
A | 9 | a0001c0001t0001g0099a0001c0001t0012g0181a0001c0001t0012g0182others(6): Show | 9 | HG02257.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+725_1122+736d others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | ||||||
chr5:60886881
|
T | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1122+559A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886881 | ||||||
chr5:60886893
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1122+547G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886893 | ||||||
chr5:60886970
|
T | G | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1122+470A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886970 | ||||||
chr5:60886984
|
G | T | 5 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(2): Show | 5 | HG01109.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122+456C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886984 | ||||||
chr5:60887061
|
C | A | 3 | a0001c0001t0007g0032a0001c0001t0007g0035a0001c0001t0007g0291 | 3 | HG02280.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1122+379G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60887061 | ||||||
chr5:60887247
|
C | T | 11 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(8): Show | 11 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1122+193G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60887247 | ||||||
chr5:60887717
|
T | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-197A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60887717 | ||||||
chr5:60887847
|
G | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1042-327C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60887847 | ||||||
chr5:60888402
|
T | C | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-882A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888402 | ||||||
chr5:60888561
|
T | A | 1 | a0001c0001t0060g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1042-1041A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888561 | ||||||
chr5:60888591
|
T | G | 1 | a0001c0001t0010g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1042-1071A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888591 | ||||||
chr5:60888701
|
T | A | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-1181A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888701 | ||||||
chr5:60888730
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0065g0144 | 2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1042-1210A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888730 | ||||||
chr5:60888762
|
C | T | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1042-1242G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888762 | ||||||
chr5:60889029
|
A | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1042-1509T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889029 | ||||||
chr5:60889029
|
A | G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-1509T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889029 | ||||||
chr5:60889069
|
C | T | 11 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(8): Show | 11 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1042-1549G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889069 | ||||||
chr5:60889429
|
C | A | 1 | a0001c0004t0001g0100 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1041+1460G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889429 | ||||||
chr5:60889456
|
C | T | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1041+1433G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889456 | ||||||
chr5:60889519
|
T | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1370A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889519 | ||||||
chr5:60889598
|
G | A | 93 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1041+1291C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889598 | ||||||
chr5:60889670
|
T | C | 1 | a0001c0001t0014g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1041+1219A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889670 | ||||||
chr5:60889955
|
C | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(289): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1041+934G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889955 | ||||||
chr5:60890005
|
C | A | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1041+884G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890005 | ||||||
chr5:60890425
|
A | T | 3 | a0001c0002t0016g0069a0001c0002t0016g0070a0001c0002t0016g0082 | 3 | HG02145.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1041+464T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890425 | ||||||
chr5:60890517
|
CCA | C | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1041+370_1041+371d others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890517 | ||||||
chr5:60890523
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1041+366T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890523 | ||||||
chr5:60890667
|
C | T | 1 | a0001c0002t0016g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1041+222G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890667 | ||||||
chr5:60890791
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1041+98G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890791 | ||||||
chr5:60891148
|
C | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.844-62G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891148 | ||||||
chr5:60891385
|
G | A | 4 | a0001c0001t0058g0262a0001c0001t0059g0263a0001c0001t0060g0019others(1): Show | 4 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-299C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891385 | ||||||
chr5:60891394
|
T | A | 4 | a0001c0001t0003g0050a0001c0001t0003g0085a0001c0001t0003g0086others(1): Show | 4 | NA18612.hp2 NA18945.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-308A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891394 | ||||||
chr5:60891442
|
T | C | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-356A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891442 | ||||||
chr5:60891469
|
T | C | 1 | a0001c0001t0011g0173 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-383A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891469 | ||||||
chr5:60891653
|
G | C | 1 | a0001c0002t0057g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.844-567C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891653 | ||||||
chr5:60891662
|
C | CT | 97 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.844-577dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891662 | ||||||
chr5:60891662
|
CT | C | 33 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(30): Show | 34 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-577delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891662 | ||||||
chr5:60892115
|
C | A | 1 | a0001c0001t0020g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.844-1029G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892115 | ||||||
chr5:60892140
|
G | GT | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(103): Show | 111 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.844-1055dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892140 | ||||||
chr5:60892245
|
C | T | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.844-1159G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892245 | ||||||
chr5:60892395
|
C | T | 94 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.844-1309G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892395 | ||||||
chr5:60892443
|
G | A | 7 | a0001c0002t0008g0065a0001c0002t0008g0079a0001c0002t0033g0048others(4): Show | 7 | HG00642.hp2 HG01069.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-1357C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892443 | ||||||
chr5:60892492
|
C | T | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.844-1406G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892492 | ||||||
chr5:60892663
|
C | T | 1 | a0001c0009t0034g0020 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.844-1577G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892663 | ||||||
chr5:60892771
|
G | A | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.844-1685C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892771 | ||||||
chr5:60892921
|
G | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-1835C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892921 | ||||||
chr5:60893199
|
G | C | 47 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(44): Show | 48 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.844-2113C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893199 | ||||||
chr5:60893479
|
C | A | 2 | a0001c0001t0002g0217a0001c0001t0009g0229 | 2 | NA19076.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.844-2393G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893479 | ||||||
chr5:60893716
|
C | A | 1 | a0001c0005t0020g0004 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.844-2630G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893716 | ||||||
chr5:60893760
|
G | A | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-2674C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893760 | ||||||
chr5:60893984
|
CT | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(236): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.844-2899delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893984 | ||||||
chr5:60894001
|
T | C | 7 | a0001c0001t0005g0250a0001c0001t0005g0251a0001c0001t0005g0255others(4): Show | 7 | HG02145.hp1 HG02886.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-2915A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894001 | ||||||
chr5:60894070
|
C | T | 23 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(20): Show | 24 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.844-2984G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894070 | ||||||
chr5:60894108
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.844-3022G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894108 | ||||||
chr5:60894135
|
C | T | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.844-3049G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894135 | ||||||
chr5:60894197
|
G | A | 1 | a0001c0001t0022g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.844-3111C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894197 | ||||||
chr5:60894250
|
C | A | 1 | a0001c0001t0003g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.844-3164G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894250 | ||||||
chr5:60894498
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0038g0163 | 2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.844-3412C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894498 | ||||||
chr5:60894579
|
T | C | 1 | a0001c0001t0007g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844-3493A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894579 | ||||||
chr5:60894603
|
G | GA | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-3518dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894603 | ||||||
chr5:60894660
|
G | T | 1 | a0001c0001t0005g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.844-3574C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894660 | ||||||
chr5:60894767
|
A | G | 37 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.843+3509T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894767 | ||||||
chr5:60894791
|
G | A | 3 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0041g0206 | 3 | HG03490.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.843+3485C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894791 | ||||||
chr5:60894937
|
G | A | 9 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0112others(6): Show | 9 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+3339C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894937 | ||||||
chr5:60894952
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.843+3324G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894952 | ||||||
chr5:60895011
|
A | G | 1 | a0001c0001t0002g0222 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843+3265T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895011 | ||||||
chr5:60895169
|
C | CA | 15 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0151others(12): Show | 15 | HG01981.hp2 HG02004.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.843+3106dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895169 | ||||||
chr5:60895169
|
CA | C | 153 | a0001c0001t0001g0147a0001c0001t0002g0005a0001c0001t0002g0036others(150): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.843+3106delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895169 | ||||||
chr5:60895368
|
C | A | 1 | a0001c0001t0063g0136 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.843+2908G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895368 | ||||||
chr5:60895633
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.843+2643T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895633 | ||||||
chr5:60895892
|
T | C | 1 | a0001c0001t0043g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.843+2384A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895892 | ||||||
chr5:60895977
|
A | ATTTCT | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.843+2294_843+2298d others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895977 | ||||||
chr5:60896007
|
C | T | 4 | a0001c0001t0012g0181a0001c0001t0012g0183a0001c0001t0012g0185others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+2269G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896007 | ||||||
chr5:60896075
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+2201G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896075 | ||||||
chr5:60896279
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.843+1997G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896279 | ||||||
chr5:60896377
|
A | AT | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.843+1898dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896377 | ||||||
chr5:60896442
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(103): Show | 111 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.843+1834G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896442 | ||||||
chr5:60896500
|
G | A | 1 | a0001c0002t0052g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.843+1776C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896500 | ||||||
chr5:60896537
|
T | G | 1 | a0001c0003t0025g0012 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.843+1739A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896537 | ||||||
chr5:60896630
|
G | A | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.843+1646C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896630 | ||||||
chr5:60896716
|
T | C | 1 | a0001c0001t0048g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.843+1560A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896716 | ||||||
chr5:60896828
|
A | G | 1 | a0001c0001t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.843+1448T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896828 | ||||||
chr5:60896840
|
T | C | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.843+1436A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896840 | ||||||
chr5:60896926
|
C | G | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.843+1350G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896926 | ||||||
chr5:60896941
|
T | C | 1 | a0001c0001t0015g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.843+1335A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896941 | ||||||
chr5:60897253
|
G | A | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.843+1023C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897253 | ||||||
chr5:60897440
|
G | C | 2 | a0001c0001t0004g0243a0001c0001t0004g0245 | 2 | HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.843+836C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897440 | ||||||
chr5:60897469
|
A | G | 4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+807T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897469 | ||||||
chr5:60897511
|
A | G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+765T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897511 | ||||||
chr5:60897512
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.843+764A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897512 | ||||||
chr5:60897527
|
A | G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+749T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897527 | ||||||
chr5:60897566
|
G | A | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.843+710C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897566 | ||||||
chr5:60897593
|
A | C | 40 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(37): Show | 41 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.843+683T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897593 | ||||||
chr5:60897951
|
T | A | 1 | a0001c0009t0034g0020 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.843+325A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897951 | ||||||
chr5:60898003
|
T | C | 1 | a0001c0001t0069g0138 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.843+273A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60898003 | ||||||
chr5:60898269
|
C | T | 1 | a0001c0001t0007g0291 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.843+7G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60898269 | ||||||
chr5:60898649
|
G | A | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.719-249C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898649 | ||||||
chr5:60898742
|
C | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-342G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898742 | ||||||
chr5:60898795
|
G | A | 1 | a0001c0001t0085g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.719-395C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898795 | ||||||
chr5:60898795
|
G | GA | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(225): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.719-396dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898795 | ||||||
chr5:60898795
|
G | GAA | 10 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(7): Show | 10 | HG01175.hp1 HG02622.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.719-397_719-396dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898795 | ||||||
chr5:60898842
|
A | G | 2 | a0001c0001t0005g0248a0001c0001t0045g0252 | 2 | HG03710.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.719-442T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898842 | ||||||
chr5:60898842
|
A | T | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.719-442T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898842 | ||||||
chr5:60899024
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.718+603A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899024 | ||||||
chr5:60899178
|
A | G | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+449T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899178 | ||||||
chr5:60899408
|
T | G | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.718+219A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899408 | ||||||
chr5:60899480
|
T | C | 1 | a0001c0002t0006g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.718+147A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899480 | ||||||
chr5:60899544
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.718+83G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899544 | ||||||
chr5:60899792
|
C | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-65G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899792 | ||||||
chr5:60899792
|
C | T | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.618-65G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899792 | ||||||
chr5:60899933
|
A | C | 4 | a0001c0001t0012g0181a0001c0001t0012g0183a0001c0001t0012g0185others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-206T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899933 | ||||||
chr5:60899950
|
C | T | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-223G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899950 | ||||||
chr5:60900187
|
T | C | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-460A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900187 | ||||||
chr5:60900383
|
G | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-656C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900383 | ||||||
chr5:60900401
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-674G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900401 | ||||||
chr5:60900448
|
G | A | 5 | a0001c0001t0007g0025a0001c0001t0010g0002a0001c0001t0010g0026others(2): Show | 6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-721C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900448 | ||||||
chr5:60900538
|
T | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(250): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.618-811A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900538 | ||||||
chr5:60900605
|
C | T | 37 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.618-878G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900605 | ||||||
chr5:60900884
|
A | C | 1 | a0001c0002t0006g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.618-1157T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900884 | ||||||
chr5:60901111
|
GTAA | G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+1328_617+1330d others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901111 | ||||||
chr5:60901252
|
C | G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+1190G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901252 | ||||||
chr5:60901273
|
T | C | 51 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.617+1169A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901273 | ||||||
chr5:60901306
|
A | C | 1 | a0001c0002t0006g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.617+1136T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901306 | ||||||
chr5:60901570
|
C | G | 1 | a0001c0001t0073g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.617+872G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901570 | ||||||
chr5:60901888
|
C | T | 51 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.617+554G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901888 | ||||||
chr5:60901895
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.617+547A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901895 | ||||||
chr5:60901963
|
AT | A | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+478delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901963 | ||||||
chr5:60902020
|
T | C | 2 | a0001c0001t0004g0243a0001c0001t0004g0245 | 2 | HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.617+422A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60902020 | ||||||
chr5:60902199
|
A | T | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.617+243T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60902199 | ||||||
chr5:60902246
|
G | A | 1 | a0001c0001t0005g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.617+196C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60902246 | ||||||
chr5:60902610
|
T | A | 1 | a0001c0001t0009g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.551-102A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60902610 | ||||||
chr5:60902686
|
G | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-178C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60902686 | ||||||
chr5:60902885
|
A | G | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.551-377T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60902885 | ||||||
chr5:60903080
|
GCTAT | G | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.550+564_550+567del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903080 | ||||||
chr5:60903374
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(244): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.550+274G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903374 | ||||||
chr5:60903536
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.550+112G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903536 | ||||||
chr5:60903556
|
A | G | 2 | a0001c0003t0025g0009a0001c0003t0026g0010 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.550+92T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903556 | ||||||
chr5:60903913
|
G | C | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-197C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60903913 | ||||||
chr5:60903919
|
T | A | 1 | a0001c0001t0004g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.482-203A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60903919 | ||||||
chr5:60904373
|
C | A | 1 | a0001c0001t0042g0037 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.481+419G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904373 | ||||||
chr5:60904439
|
T | G | 1 | a0001c0001t0079g0218 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.481+353A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904439 | ||||||
chr5:60904621
|
A | AGT | 3 | a0001c0001t0015g0282a0001c0001t0018g0270a0001c0001t0028g0039 | 3 | HG01167.hp1 HG02630.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.481+169_481+170dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | ||||||
chr5:60904621
|
AGT | A | 30 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0001g0158others(27): Show | 30 | HG00280.hp2 HG00738.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.481+169_481+170del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | ||||||
chr5:60904621
|
AGTGT | A | 17 | a0001c0001t0001g0040a0001c0001t0001g0140a0001c0001t0001g0146others(14): Show | 17 | HG01074.hp2 HG01168.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.481+167_481+170del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | ||||||
chr5:60904621
|
AGTGTGT | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0109a0001c0001t0001g0142others(10): Show | 16 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.481+165_481+170del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | ||||||
chr5:60904622
|
G | T | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+170C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904622 | ||||||
chr5:60904623
|
T | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+169A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904623 | ||||||
chr5:60904628
|
G | GTA | 3 | a0001c0001t0001g0124a0001c0001t0003g0176a0001c0001t0013g0137 | 3 | HG01433.hp1 HG04199.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.481+163_481+164ins others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(1): Show |
G | 18 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0120others(15): Show | 19 | HG01256.hp1 HG01258.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.481+156_481+163del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(3): Show |
G | 16 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0107others(13): Show | 16 | HG00639.hp1 HG02071.hp1 HG03486.hp2 others(13): Show |
intron_variant | MODIFIER | c.481+154_481+163del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(5): Show |
G | 10 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0141others(7): Show | 10 | HG02080.hp1 HG02523.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+152_481+163del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(7): Show |
G | 9 | a0001c0001t0001g0098a0001c0001t0001g0139a0001c0001t0003g0177others(6): Show | 10 | HG00673.hp1 HG02132.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+150_481+163del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(9): Show |
G | 7 | a0001c0001t0007g0018a0001c0001t0022g0286a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+148_481+163del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0007g0236a0001c0001t0042g0023 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481+146_481+163del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(13): Show |
G | 3 | a0001c0001t0007g0016a0001c0001t0010g0017a0001c0001t0042g0037 | 3 | HG01361.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481+144_481+163del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(15): Show |
G | 5 | a0001c0001t0007g0032a0001c0001t0007g0035a0001c0001t0007g0291others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+142_481+163del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(17): Show |
G | 12 | a0001c0001t0007g0015a0001c0001t0007g0024a0001c0001t0007g0025others(9): Show | 13 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.481+140_481+163del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(23): Show |
G | 4 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0060g0019others(1): Show | 4 | HG02735.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+134_481+163del others(30): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904628
|
GTGTGTGT others(27): Show |
G | 1 | a0001c0001t0059g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.481+130_481+163del others(34): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | ||||||
chr5:60904630
|
G | A | 8 | a0001c0001t0001g0124a0001c0001t0003g0176a0001c0001t0011g0093others(5): Show | 8 | HG01433.hp1 HG02056.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+162C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
G | GTA | 3 | a0001c0001t0002g0197a0001c0001t0002g0203a0001c0001t0002g0213 | 3 | HG00639.hp2 HG03490.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.481+161_481+162ins others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
GTGTGTA | G | 4 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0234others(1): Show | 4 | HG02683.hp1 NA19064.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+156_481+161del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
GTGTGTAT others(1): Show |
G | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0002g0222others(6): Show | 9 | HG00735.hp1 HG01167.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+154_481+161del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
GTGTGTAT others(3): Show |
G | 2 | a0001c0001t0002g0005a0001c0001t0009g0223 | 3 | NA18942.hp2 NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.481+152_481+161del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
GTGTGTAT others(5): Show |
G | 2 | a0001c0001t0002g0212a0001c0001t0021g0201 | 2 | HG00621.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.481+150_481+161del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
GTGTGTAT others(17): Show |
G | 1 | a0001c0007t0013g0129 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.481+138_481+161del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904630
|
GTGTGTAT others(23): Show |
G | 1 | a0001c0001t0080g0196 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.481+132_481+161del others(30): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | ||||||
chr5:60904632
|
G | A | 36 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0135others(33): Show | 36 | HG00280.hp2 HG00639.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.481+160C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | ||||||
chr5:60904632
|
GTGTA | G | 4 | a0001c0001t0002g0200a0001c0001t0003g0041a0001c0001t0003g0042others(1): Show | 4 | HG00140.hp2 NA18963.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+156_481+159del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | ||||||
chr5:60904632
|
GTGTATA | G | 3 | a0001c0001t0002g0199a0001c0001t0002g0204a0001c0001t0009g0188 | 3 | HG00735.hp2 HG01074.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.481+154_481+159del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | ||||||
chr5:60904632
|
GTGTATAT others(21): Show |
G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+132_481+159del others(28): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | ||||||
chr5:60904632
|
GTGTATAT others(29): Show |
G | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+124_481+159del others(36): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | ||||||
chr5:60904634
|
G | A | 59 | a0001c0001t0001g0040a0001c0001t0001g0114a0001c0001t0001g0124others(56): Show | 59 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.481+158C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
G | GTA | 3 | a0001c0001t0005g0246a0001c0002t0006g0178a0001c0002t0054g0044 | 3 | HG02451.hp2 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.481+156_481+157dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
G | GTATA | 3 | a0001c0001t0005g0255a0001c0001t0005g0278a0001c0002t0006g0059 | 3 | HG01884.hp1 HG02922.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.481+154_481+157dup others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0018g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.481+148_481+157dup others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0005g0251a0001c0001t0027g0257 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.481+146_481+157dup others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0005g0250a0001c0001t0005g0283 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.481+157_481+158ins others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTA | G | 4 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0028g0038others(1): Show | 4 | HG01192.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+156_481+157del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATA | G | 5 | a0001c0001t0005g0248a0001c0001t0045g0252a0001c0001t0046g0277others(2): Show | 5 | HG00642.hp1 HG01255.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+152_481+157del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(1): Show |
G | 5 | a0001c0001t0029g0264a0001c0002t0006g0056a0001c0002t0006g0060others(2): Show | 5 | HG00280.hp1 HG01496.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+150_481+157del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(3): Show |
G | 4 | a0001c0002t0006g0049a0001c0002t0006g0083a0001c0002t0006g0084others(1): Show | 4 | HG01069.hp1 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+148_481+157del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(5): Show |
G | 2 | a0001c0002t0016g0082a0001c0002t0052g0022 | 2 | HG02809.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.481+146_481+157del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(7): Show |
G | 5 | a0001c0002t0008g0080a0001c0002t0016g0069a0001c0002t0017g0045others(2): Show | 5 | HG00140.hp1 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+144_481+157del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(9): Show |
G | 13 | a0001c0002t0008g0046a0001c0002t0008g0047a0001c0002t0008g0065others(10): Show | 13 | HG00642.hp2 HG00738.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.481+142_481+157del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(11): Show |
G | 2 | a0001c0002t0016g0064a0001c0002t0032g0067 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.481+140_481+157del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(15): Show |
G | 3 | a0001c0001t0004g0245a0001c0001t0018g0247a0001c0002t0017g0072 | 3 | HG01175.hp2 HG02004.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.481+136_481+157del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(17): Show |
G | 14 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(11): Show | 15 | HG00673.hp2 HG02132.hp2 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+134_481+157del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904634
|
GTATATAT others(29): Show |
G | 1 | a0001c0001t0029g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+122_481+157del others(36): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | ||||||
chr5:60904636
|
A | G | 1 | a0001c0001t0028g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.481+156T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904636 | ||||||
chr5:60904638
|
A | G | 1 | a0001c0001t0028g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+154T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904638 | ||||||
chr5:60904658
|
A | G | 1 | a0001c0001t0018g0247 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.481+134T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904658 | ||||||
chr5:60904666
|
A | G | 1 | a0001c0001t0009g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481+126T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904666 | ||||||
chr5:60904668
|
A | G | 1 | a0001c0001t0009g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481+124T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904668 | ||||||
chr5:60904683
|
T | A | 1 | a0001c0001t0002g0036 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.481+109A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904683 | ||||||
chr5:60904685
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481+107T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904685 | ||||||
chr5:60904915
|
T | C | 6 | a0001c0003t0024g0007a0001c0003t0024g0008a0001c0003t0025g0009others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-42A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60904915 | ||||||
chr5:60904929
|
T | A | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.400-56A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60904929 | ||||||
chr5:60905029
|
A | T | 4 | a0001c0003t0025g0009a0001c0003t0025g0012a0001c0003t0026g0010others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-156T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905029 | ||||||
chr5:60905166
|
G | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-293C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905166 | ||||||
chr5:60905285
|
TTTCAG | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(117): Show | 125 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.400-417_400-413del others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905285 | ||||||
chr5:60905300
|
A | G | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.400-427T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905300 | ||||||
chr5:60905498
|
T | C | 4 | a0001c0001t0020g0108a0001c0001t0037g0191a0001c0001t0037g0192others(1): Show | 5 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-625A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905498 | ||||||
chr5:60905877
|
G | A | 2 | a0001c0002t0033g0048a0001c0002t0033g0071 | 2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.400-1004C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905877 | ||||||
chr5:60905888
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(244): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.400-1015A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905888 | ||||||
chr5:60905950
|
C | G | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.400-1077G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905950 | ||||||
chr5:60905953
|
C | G | 2 | a0001c0001t0039g0123a0001c0004t0039g0161 | 2 | NA19076.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.400-1080G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905953 | ||||||
chr5:60906076
|
C | T | 1 | a0001c0002t0006g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.400-1203G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906076 | ||||||
chr5:60906163
|
T | C | 1 | a0001c0001t0023g0284 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-1290A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906163 | ||||||
chr5:60906217
|
G | A | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.400-1344C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906217 | ||||||
chr5:60906350
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.400-1477A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906350 | ||||||
chr5:60906418
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.400-1545C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906418 | ||||||
chr5:60906420
|
A | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(104): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.400-1547T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906420 | ||||||
chr5:60906587
|
G | T | 1 | a0001c0001t0014g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.400-1714C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906587 | ||||||
chr5:60906710
|
C | T | 1 | a0001c0001t0065g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.400-1837G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906710 | ||||||
chr5:60906730
|
AAAAT | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.400-1861_400-1858d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906730 | ||||||
chr5:60906758
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.400-1885A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906758 | ||||||
chr5:60906812
|
A | G | 1 | a0001c0001t0071g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.400-1939T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906812 | ||||||
chr5:60906912
|
T | C | 9 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0112others(6): Show | 9 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-2039A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906912 | ||||||
chr5:60907029
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.400-2156A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907029 | ||||||
chr5:60907079
|
A | G | 51 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.400-2206T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907079 | ||||||
chr5:60907150
|
C | T | 1 | a0001c0001t0007g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400-2277G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907150 | ||||||
chr5:60907168
|
C | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-2295G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907168 | ||||||
chr5:60907186
|
A | G | 1 | a0001c0001t0013g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.400-2313T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907186 | ||||||
chr5:60907303
|
C | T | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-2430G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907303 | ||||||
chr5:60907355
|
C | CT | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.400-2483dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907355 | ||||||
chr5:60907355
|
C | CTTT | 28 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(25): Show | 29 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.400-2485_400-2483d others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907355 | ||||||
chr5:60907387
|
C | G | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0118 | 3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.400-2514G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907387 | ||||||
chr5:60907388
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0155 | 2 | NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.400-2515A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907388 | ||||||
chr5:60907513
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0141others(1): Show | 4 | NA18973.hp1 NA19054.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-2640G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907513 | ||||||
chr5:60907532
|
T | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.400-2659A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907532 | ||||||
chr5:60907543
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.400-2670T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907543 | ||||||
chr5:60907640
|
A | T | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.400-2767T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907640 | ||||||
chr5:60908310
|
C | A | 2 | a0001c0001t0005g0248a0001c0001t0045g0252 | 2 | HG03710.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.400-3437G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908310 | ||||||
chr5:60908359
|
G | C | 6 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-3486C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908359 | ||||||
chr5:60908391
|
A | G | 1 | a0001c0001t0074g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.400-3518T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908391 | ||||||
chr5:60908533
|
C | G | 2 | a0001c0001t0001g0166a0001c0001t0011g0149 | 2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.400-3660G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908533 | ||||||
chr5:60908564
|
C | CAT | 3 | a0001c0001t0059g0263a0001c0002t0017g0045a0001c0002t0052g0022 | 3 | HG01099.hp1 HG01175.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.400-3693_400-3692d others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908564 | ||||||
chr5:60908564
|
C | CATAT | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-3695_400-3692d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908564 | ||||||
chr5:60908579
|
A | AT | 7 | a0001c0001t0001g0142a0001c0001t0022g0286a0001c0001t0022g0288others(4): Show | 7 | HG01256.hp2 HG02071.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-3707dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908579 | ||||||
chr5:60908581
|
A | AT | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0094others(56): Show | 64 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.400-3709dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | ||||||
chr5:60908581
|
A | ATT | 6 | a0001c0001t0002g0200a0001c0001t0034g0051a0001c0001t0058g0262others(3): Show | 6 | HG00140.hp2 HG02735.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-3709_400-3708i others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | ||||||
chr5:60908581
|
A | ATTT | 35 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(32): Show | 36 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.400-3709_400-3708i others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | ||||||
chr5:60908581
|
A | T | 8 | a0001c0001t0001g0142a0001c0001t0022g0286a0001c0001t0022g0288others(5): Show | 8 | HG01256.hp2 HG02071.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-3708T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | ||||||
chr5:60908583
|
A | AT | 37 | a0001c0001t0001g0139a0001c0001t0001g0166a0001c0001t0003g0041others(34): Show | 37 | HG00280.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.400-3711dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908583 | ||||||
chr5:60908583
|
A | ATTTT | 12 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0002g0226others(9): Show | 12 | HG03710.hp2 NA18940.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.400-3714_400-3711d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908583 | ||||||
chr5:60908583
|
A | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(115): Show | 124 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.400-3710T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908583 | ||||||
chr5:60908584
|
T | TA | 24 | a0001c0001t0001g0140a0001c0001t0003g0168a0001c0001t0003g0169others(21): Show | 25 | HG01074.hp2 HG01255.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.400-3712_400-3711i others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908584 | ||||||
chr5:60908585
|
T | A | 4 | a0001c0001t0005g0278a0001c0001t0018g0066a0001c0001t0018g0270others(1): Show | 4 | HG01167.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-3712A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908585 | ||||||
chr5:60908586
|
T | A | 12 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(9): Show | 12 | HG01361.hp1 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-3713A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908586 | ||||||
chr5:60908649
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.400-3776G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908649 | ||||||
chr5:60908676
|
G | C | 1 | a0001c0002t0056g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.400-3803C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908676 | ||||||
chr5:60908696
|
AG | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-3824delC | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908696 | ||||||
chr5:60908704
|
CATT | C | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.400-3834_400-3832d others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908704 | ||||||
chr5:60908759
|
T | A | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400-3886A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908759 | ||||||
chr5:60908769
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.400-3896G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908769 | ||||||
chr5:60908891
|
A | T | 4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4018T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908891 | ||||||
chr5:60908900
|
T | C | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.400-4027A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908900 | ||||||
chr5:60909094
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0141 | 2 | NA19054.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.400-4221A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909094 | ||||||
chr5:60909114
|
T | A | 1 | a0001c0001t0005g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.400-4241A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909114 | ||||||
chr5:60909196
|
A | G | 4 | a0001c0001t0001g0124a0001c0001t0013g0126a0001c0001t0035g0127others(1): Show | 4 | HG01433.hp1 HG01928.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4323T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909196 | ||||||
chr5:60909243
|
G | GAAAAAAA others(1): Show |
13 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0240others(10): Show | 13 | HG01517.hp2 HG02004.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-4378_400-4371d others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAAAAAA others(2): Show |
5 | a0001c0001t0004g0006a0001c0001t0004g0244a0001c0001t0004g0273others(2): Show | 6 | HG00673.hp2 HG01361.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-4379_400-4371d others(11): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAAAAAA others(3): Show |
3 | a0001c0001t0007g0236a0001c0001t0010g0029a0001c0001t0027g0257 | 3 | HG02258.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.400-4380_400-4371d others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAAAAAA others(4): Show |
12 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0031others(9): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-4381_400-4371d others(13): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAAAAAA others(5): Show |
4 | a0001c0001t0007g0018a0001c0001t0007g0025a0001c0001t0007g0032others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-4382_400-4371d others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAAAAAA others(6): Show |
1 | a0001c0001t0010g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.400-4383_400-4371d others(15): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAAAAAA others(9): Show |
2 | a0001c0001t0007g0024a0001c0001t0010g0034 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.400-4386_400-4371d others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
G | GAAGAAAA others(3): Show |
4 | a0001c0003t0025g0009a0001c0003t0025g0012a0001c0003t0026g0010others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4371_400-4370i others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
GAAAA | G | 38 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0116others(35): Show | 38 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.400-4374_400-4371d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
GAAAAA | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(99): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.400-4375_400-4371d others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
GAAAAAA | G | 55 | a0001c0001t0001g0109a0001c0001t0001g0120a0001c0001t0001g0125others(52): Show | 56 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.400-4376_400-4371d others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
GAAAAAAA | G | 12 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0005g0250others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.400-4377_400-4371d others(9): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909243
|
GAAAAAAA others(14): Show |
G | 3 | a0001c0001t0037g0191a0001c0001t0037g0192a0001c0005t0020g0004 | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4391_400-4371d others(23): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | ||||||
chr5:60909278
|
A | G | 4 | a0001c0003t0025g0009a0001c0003t0025g0012a0001c0003t0026g0010others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4405T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909278 | ||||||
chr5:60909706
|
C | T | 1 | a0001c0002t0017g0045 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.400-4833G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909706 | ||||||
chr5:60909910
|
C | T | 1 | a0001c0002t0016g0064 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.400-5037G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909910 | ||||||
chr5:60909935
|
T | C | 1 | a0001c0001t0045g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.400-5062A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909935 | ||||||
chr5:60909961
|
GA | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(7): Show | 10 | HG00642.hp2 HG01884.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-5089delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909961 | ||||||
chr5:60909972
|
A | T | 75 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(72): Show | 76 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.400-5099T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909972 | ||||||
chr5:60909974
|
AT | A | 19 | a0001c0002t0008g0046a0001c0002t0008g0047a0001c0002t0008g0065others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.400-5102delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909974 | ||||||
chr5:60909975
|
T | A | 34 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(31): Show | 35 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.400-5102A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909975 | ||||||
chr5:60909978
|
T | A | 1 | a0001c0002t0017g0078 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.400-5105A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909978 | ||||||
chr5:60910195
|
T | A | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.400-5322A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910195 | ||||||
chr5:60910295
|
T | C | 1 | a0001c0001t0005g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.400-5422A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910295 | ||||||
chr5:60910298
|
A | G | 9 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0112others(6): Show | 9 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-5425T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910298 | ||||||
chr5:60910850
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.400-5977G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910850 | ||||||
chr5:60911139
|
C | T | 2 | a0001c0001t0037g0191a0001c0001t0037g0192 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.400-6266G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911139 | ||||||
chr5:60911262
|
T | C | 1 | a0001c0001t0003g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.400-6389A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911262 | ||||||
chr5:60911304
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.400-6431A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911304 | ||||||
chr5:60911397
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00639.hp1 HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.400-6524A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911397 | ||||||
chr5:60911436
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0003g0177 | 2 | NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400-6563C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911436 | ||||||
chr5:60911438
|
G | T | 6 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(3): Show | 6 | HG01109.hp1 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-6565C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911438 | ||||||
chr5:60911438
|
GT | G | 6 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-6566delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911438 | ||||||
chr5:60911615
|
T | C | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.399+6650A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911615 | ||||||
chr5:60911774
|
GT | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(244): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.399+6490delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911774 | ||||||
chr5:60911791
|
G | T | 2 | a0001c0001t0027g0256a0001c0001t0027g0257 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.399+6474C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911791 | ||||||
chr5:60912267
|
T | G | 1 | a0001c0001t0014g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.399+5998A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912267 | ||||||
chr5:60912498
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0009g0207 | 2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.399+5767G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912498 | ||||||
chr5:60912601
|
T | G | 1 | a0001c0001t0043g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.399+5664A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912601 | ||||||
chr5:60912650
|
G | A | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.399+5615C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912650 | ||||||
chr5:60912650
|
G | C | 1 | a0001c0001t0082g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.399+5615C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912650 | ||||||
chr5:60912769
|
A | C | 6 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+5496T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912769 | ||||||
chr5:60912854
|
C | T | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+5411G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912854 | ||||||
chr5:60912978
|
G | T | 51 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.399+5287C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912978 | ||||||
chr5:60913143
|
A | T | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+5122T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60913143 | ||||||
chr5:60913339
|
G | T | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+4926C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60913339 | ||||||
chr5:60913888
|
C | T | 1 | a0001c0001t0070g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.399+4377G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60913888 | ||||||
chr5:60914168
|
T | A | 2 | a0001c0001t0005g0268a0001c0001t0018g0247 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.399+4097A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914168 | ||||||
chr5:60914204
|
C | T | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.399+4061G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914204 | ||||||
chr5:60914304
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(207): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.399+3961C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914304 | ||||||
chr5:60914595
|
G | A | 4 | a0001c0002t0006g0049a0001c0002t0006g0060a0001c0002t0006g0083others(1): Show | 4 | HG01981.hp1 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+3670C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914595 | ||||||
chr5:60914605
|
G | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+3660C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914605 | ||||||
chr5:60914713
|
G | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+3552C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914713 | ||||||
chr5:60914744
|
G | A | 1 | a0001c0001t0020g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.399+3521C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914744 | ||||||
chr5:60914789
|
T | TA | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(116): Show | 124 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.399+3475dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914789 | ||||||
chr5:60914789
|
TA | T | 17 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0005g0248others(14): Show | 17 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.399+3475delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914789 | ||||||
chr5:60914810
|
G | C | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+3455C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914810 | ||||||
chr5:60914844
|
A | G | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.399+3421T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914844 | ||||||
chr5:60914901
|
T | C | 8 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0002g0202others(5): Show | 8 | HG03490.hp2 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+3364A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914901 | ||||||
chr5:60915002
|
A | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+3263T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915002 | ||||||
chr5:60915046
|
C | G | 1 | a0001c0001t0009g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.399+3219G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915046 | ||||||
chr5:60915109
|
A | G | 43 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(40): Show | 44 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.399+3156T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915109 | ||||||
chr5:60915137
|
T | A | 1 | a0001c0001t0005g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.399+3128A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915137 | ||||||
chr5:60915194
|
G | T | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.399+3071C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915194 | ||||||
chr5:60915565
|
A | G | 1 | a0001c0001t0003g0172 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.399+2700T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915565 | ||||||
chr5:60915598
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.399+2667A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915598 | ||||||
chr5:60915657
|
T | C | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+2608A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915657 | ||||||
chr5:60915669
|
A | G | 14 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+2596T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915669 | ||||||
chr5:60915819
|
C | A | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.399+2446G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915819 | ||||||
chr5:60915825
|
C | A | 2 | a0001c0001t0002g0200a0001c0001t0009g0189 | 2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.399+2440G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915825 | ||||||
chr5:60916274
|
A | G | 1 | a0001c0001t0031g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.399+1991T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916274 | ||||||
chr5:60916493
|
T | C | 1 | a0001c0001t0028g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+1772A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916493 | ||||||
chr5:60916507
|
A | G | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.399+1758T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916507 | ||||||
chr5:60916623
|
T | A | 1 | a0001c0001t0037g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.399+1642A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916623 | ||||||
chr5:60916736
|
T | G | 2 | a0001c0003t0024g0007a0001c0003t0024g0008 | 2 | HG01109.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.399+1529A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916736 | ||||||
chr5:60917065
|
G | A | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.399+1200C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917065 | ||||||
chr5:60917317
|
C | T | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+948G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917317 | ||||||
chr5:60917370
|
A | G | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+895T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917370 | ||||||
chr5:60917436
|
T | G | 1 | a0001c0001t0041g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.399+829A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917436 | ||||||
chr5:60917516
|
T | C | 2 | a0001c0001t0042g0023a0001c0001t0042g0037 | 2 | HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.399+749A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917516 | ||||||
chr5:60917588
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.399+677A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917588 | ||||||
chr5:60917657
|
T | C | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+608A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917657 | ||||||
chr5:60917779
|
A | G | 1 | a0001c0001t0007g0291 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.399+486T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917779 | ||||||
chr5:60918134
|
T | G | 3 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0043 | 3 | NA18963.hp1 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.399+131A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60918134 | ||||||
chr5:60918142
|
A | C | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.399+123T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60918142 | ||||||
chr5:60918432
|
G | T | 1 | a0001c0001t0010g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276-44C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918432 | ||||||
chr5:60918482
|
G | A | 1 | a0001c0002t0008g0079 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.276-94C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918482 | ||||||
chr5:60918513
|
T | C | 1 | a0001c0001t0003g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.276-125A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918513 | ||||||
chr5:60918622
|
G | T | 1 | a0001c0001t0085g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.276-234C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918622 | ||||||
chr5:60918676
|
T | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(288): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.276-288A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918676 | ||||||
chr5:60918920
|
A | C | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.276-532T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918920 | ||||||
chr5:60918922
|
C | T | 1 | a0001c0001t0049g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.276-534G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918922 | ||||||
chr5:60918929
|
T | C | 1 | a0001c0001t0042g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.276-541A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918929 | ||||||
chr5:60919062
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.276-674T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919062 | ||||||
chr5:60919089
|
C | T | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.276-701G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919089 | ||||||
chr5:60919216
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.276-828G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919216 | ||||||
chr5:60919229
|
G | A | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276-841C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919229 | ||||||
chr5:60919344
|
T | C | 1 | a0001c0004t0001g0143 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.276-956A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919344 | ||||||
chr5:60919353
|
G | C | 1 | a0001c0001t0029g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.276-965C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919353 | ||||||
chr5:60919412
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.276-1024A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919412 | ||||||
chr5:60919500
|
C | T | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.276-1112G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919500 | ||||||
chr5:60919557
|
A | T | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.276-1169T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919557 | ||||||
chr5:60919644
|
T | C | 1 | a0001c0001t0080g0196 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.276-1256A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919644 | ||||||
chr5:60919654
|
A | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.276-1266T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919654 | ||||||
chr5:60919894
|
G | C | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.276-1506C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919894 | ||||||
chr5:60919977
|
A | G | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276-1589T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919977 | ||||||
chr5:60920089
|
G | A | 4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.276-1701C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920089 | ||||||
chr5:60920216
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.276-1828A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920216 | ||||||
chr5:60920577
|
T | C | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.275+1477A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920577 | ||||||
chr5:60920757
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.275+1297G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920757 | ||||||
chr5:60920806
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(244): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.275+1248G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920806 | ||||||
chr5:60920997
|
G | A | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.275+1057C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920997 | ||||||
chr5:60921001
|
C | T | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.275+1053G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921001 | ||||||
chr5:60921150
|
C | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0204others(1): Show | 4 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.275+904G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921150 | ||||||
chr5:60921211
|
G | A | 51 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.275+843C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921211 | ||||||
chr5:60921600
|
T | C | 6 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(3): Show | 6 | HG02809.hp1 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+454A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921600 | ||||||
chr5:60921612
|
T | C | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+442A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921612 | ||||||
chr5:60921660
|
T | C | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+394A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921660 | ||||||
chr5:60921733
|
A | T | 1 | a0001c0002t0006g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.275+321T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921733 | ||||||
chr5:60921824
|
A | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(244): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.275+230T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921824 | ||||||
chr5:60921841
|
C | A | 1 | a0001c0001t0002g0210 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.275+213G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921841 | ||||||
chr5:60922592
|
G | A | 1 | a0001c0001t0043g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.174-437C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60922592 | ||||||
chr5:60922843
|
T | C | 1 | a0001c0001t0003g0171 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.174-688A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60922843 | ||||||
chr5:60923019
|
C | T | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.174-864G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923019 | ||||||
chr5:60923095
|
T | TG | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(207): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.174-941dupC | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923095 | ||||||
chr5:60923224
|
A | G | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.174-1069T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923224 | ||||||
chr5:60923541
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.174-1386T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923541 | ||||||
chr5:60923653
|
A | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(251): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.174-1498T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923653 | ||||||
chr5:60923669
|
A | T | 4 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-1514T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923669 | ||||||
chr5:60923919
|
A | G | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-1764T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923919 | ||||||
chr5:60923973
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.174-1818C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923973 | ||||||
chr5:60924051
|
T | A | 1 | a0001c0001t0022g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.174-1896A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924051 | ||||||
chr5:60924267
|
C | T | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.174-2112G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924267 | ||||||
chr5:60924597
|
A | G | 1 | a0001c0002t0006g0060 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.174-2442T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924597 | ||||||
chr5:60924813
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.174-2658C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924813 | ||||||
chr5:60924834
|
C | T | 1 | a0001c0001t0013g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.174-2679G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924834 | ||||||
chr5:60924923
|
T | C | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174-2768A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924923 | ||||||
chr5:60924932
|
T | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-2777A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924932 | ||||||
chr5:60925102
|
C | T | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-2947G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925102 | ||||||
chr5:60925204
|
C | T | 1 | a0001c0001t0007g0291 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.174-3049G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925204 | ||||||
chr5:60925394
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.174-3239G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925394 | ||||||
chr5:60925467
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(250): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.174-3312C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925467 | ||||||
chr5:60925965
|
G | A | 1 | a0001c0001t0065g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.173+2899C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925965 | ||||||
chr5:60925970
|
C | T | 1 | a0001c0001t0031g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.173+2894G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925970 | ||||||
chr5:60926013
|
C | T | 2 | a0001c0001t0034g0051a0001c0001t0060g0019 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173+2851G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926013 | ||||||
chr5:60926071
|
C | T | 2 | a0001c0001t0003g0104a0001c0001t0003g0105 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.173+2793G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926071 | ||||||
chr5:60926077
|
G | A | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.173+2787C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926077 | ||||||
chr5:60926132
|
T | C | 4 | a0001c0003t0025g0009a0001c0003t0025g0012a0001c0003t0026g0010others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+2732A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926132 | ||||||
chr5:60926216
|
A | G | 1 | a0001c0001t0049g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.173+2648T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926216 | ||||||
chr5:60926296
|
C | T | 1 | a0001c0001t0021g0221 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.173+2568G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926296 | ||||||
chr5:60926342
|
T | C | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.173+2522A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926342 | ||||||
chr5:60926575
|
T | C | 1 | a0001c0001t0018g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.173+2289A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926575 | ||||||
chr5:60927182
|
C | T | 1 | a0001c0001t0011g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.173+1682G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927182 | ||||||
chr5:60927337
|
T | C | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.173+1527A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927337 | ||||||
chr5:60927384
|
T | G | 1 | a0001c0001t0003g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.173+1480A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927384 | ||||||
chr5:60927546
|
G | A | 1 | a0001c0001t0023g0289 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.173+1318C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927546 | ||||||
chr5:60927695
|
C | T | 1 | a0001c0001t0045g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.173+1169G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927695 | ||||||
chr5:60927706
|
T | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+1158A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927706 | ||||||
chr5:60927736
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.173+1128T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927736 | ||||||
chr5:60927914
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.173+950T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927914 | ||||||
chr5:60928029
|
C | G | 37 | a0001c0001t0018g0066a0001c0002t0006g0049a0001c0002t0006g0056others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.173+835G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928029 | ||||||
chr5:60928618
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.173+246G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928618 | ||||||
chr5:60928715
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+149G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928715 | ||||||
chr5:60928731
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0145a0001c0001t0001g0146 | 4 | NA18940.hp1 NA18942.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+133G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928731 | ||||||
chr5:60929069
|
T | G | 1 | a0001c0001t0042g0037 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.78-110A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929069 | ||||||
chr5:60929087
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.78-128G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929087 | ||||||
chr5:60929190
|
C | T | 2 | a0001c0001t0037g0191a0001c0001t0037g0192 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.78-231G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929190 | ||||||
chr5:60929465
|
G | A | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-506C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929465 | ||||||
chr5:60929696
|
A | G | 9 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0198others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-737T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929696 | ||||||
chr5:60929783
|
T | C | 1 | a0001c0002t0016g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.78-824A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929783 | ||||||
chr5:60930205
|
G | A | 1 | a0001c0001t0010g0033 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.78-1246C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930205 | ||||||
chr5:60930214
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.78-1255T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930214 | ||||||
chr5:60930325
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.78-1366C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930325 | ||||||
chr5:60930556
|
T | TAAAAAC | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(287): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.78-1603_78-1598dup others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930556 | ||||||
chr5:60930578
|
C | G | 1 | a0001c0001t0002g0222 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-1619G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930578 | ||||||
chr5:60930759
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.78-1800A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930759 | ||||||
chr5:60930888
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.78-1929G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930888 | ||||||
chr5:60930926
|
G | A | 1 | a0001c0001t0013g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.78-1967C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930926 | ||||||
chr5:60931119
|
C | CA | 9 | a0001c0001t0005g0248a0001c0001t0005g0275a0001c0001t0028g0038others(6): Show | 9 | HG01516.hp2 HG01517.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-2161dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931119 | ||||||
chr5:60931194
|
G | T | 1 | a0001c0001t0021g0221 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.78-2235C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931194 | ||||||
chr5:60931303
|
T | A | 1 | a0001c0001t0005g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.78-2344A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931303 | ||||||
chr5:60931570
|
A | T | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-2611T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931570 | ||||||
chr5:60931600
|
C | T | 1 | a0001c0001t0072g0097 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.78-2641G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931600 | ||||||
chr5:60931790
|
A | G | 1 | a0001c0001t0012g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.78-2831T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931790 | ||||||
chr5:60932096
|
A | G | 51 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.78-3137T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932096 | ||||||
chr5:60932189
|
A | C | 21 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(18): Show | 22 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.78-3230T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932189 | ||||||
chr5:60932196
|
A | C | 1 | a0001c0001t0038g0163 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.78-3237T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932196 | ||||||
chr5:60932252
|
T | C | 1 | a0001c0001t0077g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-3293A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932252 | ||||||
chr5:60932331
|
G | T | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.78-3372C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932331 | ||||||
chr5:60932627
|
A | G | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-3668T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932627 | ||||||
chr5:60932688
|
TCA | T | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-3731_78-3730del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932688 | ||||||
chr5:60932789
|
A | G | 8 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0002g0202others(5): Show | 8 | HG03490.hp2 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-3830T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932789 | ||||||
chr5:60932792
|
G | A | 14 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-3833C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932792 | ||||||
chr5:60932908
|
G | C | 1 | a0001c0001t0011g0149 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.78-3949C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932908 | ||||||
chr5:60933160
|
T | C | 1 | a0001c0001t0034g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.78-4201A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933160 | ||||||
chr5:60933215
|
T | C | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.78-4256A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933215 | ||||||
chr5:60933216
|
C | CT | 35 | a0001c0001t0004g0240a0001c0001t0015g0259a0001c0001t0018g0066others(32): Show | 35 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.78-4258dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | ||||||
chr5:60933216
|
C | T | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.78-4257G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | ||||||
chr5:60933216
|
CT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(175): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.78-4258delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | ||||||
chr5:60933216
|
CTT | C | 14 | a0001c0001t0001g0150a0001c0001t0002g0197a0001c0001t0012g0181others(11): Show | 14 | HG01175.hp1 HG02615.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-4259_78-4258del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | ||||||
chr5:60933222
|
T | C | 12 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(9): Show | 12 | HG01175.hp1 HG02735.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-4263A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933222 | ||||||
chr5:60933238
|
A | T | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-4279T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933238 | ||||||
chr5:60933323
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0162 | 2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.78-4364T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933323 | ||||||
chr5:60933340
|
A | C | 1 | a0001c0001t0009g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.78-4381T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933340 | ||||||
chr5:60933436
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.78-4477G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933436 | ||||||
chr5:60933439
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(204): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.78-4480T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933439 | ||||||
chr5:60933642
|
T | G | 6 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(3): Show | 6 | HG02622.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-4683A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933642 | ||||||
chr5:60933772
|
T | C | 1 | a0001c0001t0047g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78-4813A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933772 | ||||||
chr5:60933938
|
T | TAC | 3 | a0001c0001t0018g0270a0001c0001t0085g0180a0001c0002t0016g0064 | 3 | HG01167.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.78-4981_78-4980dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933938 | ||||||
chr5:60933938
|
T | TACACAC | 42 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0195others(39): Show | 43 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.78-4985_78-4980dup others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933938 | ||||||
chr5:60933938
|
T | TACACACA others(1): Show |
9 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0198others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-4987_78-4980dup others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933938 | ||||||
chr5:60934389
|
G | A | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0118 | 3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.78-5430C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934389 | ||||||
chr5:60934487
|
T | C | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-5528A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934487 | ||||||
chr5:60934494
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(204): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.78-5535C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934494 | ||||||
chr5:60934504
|
T | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0001g0151others(2): Show | 5 | NA18957.hp2 NA18961.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-5545A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934504 | ||||||
chr5:60934523
|
T | C | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.78-5564A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934523 | ||||||
chr5:60934600
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.78-5641C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934600 | ||||||
chr5:60934758
|
A | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-5799T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934758 | ||||||
chr5:60934886
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.78-5927G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934886 | ||||||
chr5:60935104
|
G | T | 1 | a0001c0001t0014g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78-6145C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935104 | ||||||
chr5:60935130
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.78-6171A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935130 | ||||||
chr5:60935259
|
G | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-6300C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935259 | ||||||
chr5:60935354
|
T | C | 1 | a0001c0002t0052g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.78-6395A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935354 | ||||||
chr5:60935797
|
A | G | 1 | a0001c0001t0047g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78-6838T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935797 | ||||||
chr5:60935867
|
C | A | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.78-6908G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935867 | ||||||
chr5:60935910
|
A | G | 29 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(26): Show | 30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-6951T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935910 | ||||||
chr5:60935993
|
G | C | 1 | a0001c0002t0033g0048 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78-7034C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935993 | ||||||
chr5:60936316
|
T | C | 1 | a0001c0001t0036g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.78-7357A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936316 | ||||||
chr5:60936483
|
A | T | 1 | a0001c0001t0020g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-7524T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936483 | ||||||
chr5:60936515
|
A | G | 38 | a0001c0001t0018g0066a0001c0002t0006g0049a0001c0002t0006g0056others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.78-7556T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936515 | ||||||
chr5:60936564
|
G | A | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.78-7605C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936564 | ||||||
chr5:60936710
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(245): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.78-7751G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936710 | ||||||
chr5:60936749
|
T | C | 1 | a0001c0001t0005g0271 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78-7790A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936749 | ||||||
chr5:60936928
|
C | T | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.78-7969G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936928 | ||||||
chr5:60936942
|
T | C | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.78-7983A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936942 | ||||||
chr5:60937148
|
G | A | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+7784C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937148 | ||||||
chr5:60937709
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.77+7223A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937709 | ||||||
chr5:60937748
|
C | T | 1 | a0001c0001t0011g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.77+7184G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937748 | ||||||
chr5:60937859
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.77+7073C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937859 | ||||||
chr5:60938009
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(196): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.77+6923C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938009 | ||||||
chr5:60938011
|
G | A | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+6921C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938011 | ||||||
chr5:60938024
|
TATACATA others(1): Show |
T | 4 | a0001c0001t0002g0210a0001c0001t0009g0190a0001c0001t0081g0220others(1): Show | 4 | HG00735.hp1 HG02602.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6900_77+6907del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938024 | ||||||
chr5:60938040
|
C | T | 4 | a0001c0001t0022g0286a0001c0001t0023g0284a0001c0001t0023g0285others(1): Show | 4 | HG03139.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6892G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(3): Show |
C | 14 | a0001c0001t0002g0005a0001c0001t0002g0195a0001c0001t0002g0197others(11): Show | 15 | HG03831.hp2 NA18939.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+6882_77+6891del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(5): Show |
C | 4 | a0001c0001t0002g0202a0001c0001t0002g0228a0001c0001t0002g0231others(1): Show | 4 | HG03491.hp1 HG03927.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6880_77+6891del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(7): Show |
C | 4 | a0001c0001t0002g0203a0001c0001t0042g0023a0001c0001t0042g0037others(1): Show | 4 | HG01361.hp1 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+6878_77+6891del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(9): Show |
C | 4 | a0001c0001t0001g0109a0001c0001t0007g0035a0001c0001t0010g0026others(1): Show | 4 | HG02886.hp2 HG02922.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6876_77+6891del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(11): Show |
C | 24 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(21): Show | 25 | HG00621.hp1 HG00639.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.77+6874_77+6891del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(13): Show |
C | 15 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0007g0015others(12): Show | 15 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+6872_77+6891del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(15): Show |
C | 8 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0010g0034others(5): Show | 8 | HG02071.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.77+6870_77+6891del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(17): Show |
C | 14 | a0001c0001t0003g0168a0001c0001t0003g0169a0001c0001t0003g0170others(11): Show | 15 | HG01255.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+6868_77+6891del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938040
|
CATACATA others(19): Show |
C | 2 | a0001c0001t0009g0229a0001c0001t0012g0184 | 2 | HG02818.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.77+6866_77+6891del others(26): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | ||||||
chr5:60938042
|
TACATAC | T | 14 | a0001c0001t0002g0036a0001c0001t0002g0193a0001c0001t0002g0198others(11): Show | 14 | HG00738.hp2 HG01099.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+6884_77+6889del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938042 | ||||||
chr5:60938044
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(81): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.77+6888G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | ||||||
chr5:60938044
|
CATACATA others(1): Show |
C | 5 | a0001c0001t0029g0264a0001c0003t0025g0009a0001c0003t0025g0012others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+6880_77+6887del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | ||||||
chr5:60938044
|
CATACATA others(7): Show |
C | 1 | a0001c0002t0006g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.77+6874_77+6887del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | ||||||
chr5:60938044
|
CATACATA others(9): Show |
C | 1 | a0001c0002t0016g0064 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.77+6872_77+6887del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | ||||||
chr5:60938044
|
CATACATA others(11): Show |
C | 1 | a0001c0002t0008g0065 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.77+6870_77+6887del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | ||||||
chr5:60938048
|
C | CAT | 8 | a0001c0001t0004g0245a0001c0001t0004g0272a0001c0001t0004g0273others(5): Show | 8 | HG00673.hp2 HG02004.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+6882_77+6883dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
C | CATAT | 8 | a0001c0001t0004g0238a0001c0001t0004g0240a0001c0001t0004g0241others(5): Show | 8 | HG02273.hp1 HG02965.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.77+6880_77+6883dup others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
C | CATATAT | 3 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0031g0239 | 4 | HG02132.hp2 NA18973.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6878_77+6883dup others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(130): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.77+6884G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
CAT | C | 5 | a0001c0001t0005g0246a0001c0001t0005g0255a0001c0001t0005g0280others(2): Show | 5 | HG02451.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6882_77+6883del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0015g0282 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.77+6874_77+6883del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
CATATATA others(11): Show |
C | 2 | a0001c0001t0027g0256a0001c0001t0027g0257 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.77+6866_77+6883del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938048
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0005g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.77+6860_77+6883del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | ||||||
chr5:60938052
|
T | C | 3 | a0001c0001t0005g0248a0001c0001t0050g0281a0001c0001t0051g0269 | 3 | HG00099.hp1 HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.77+6880A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938052 | ||||||
chr5:60938063
|
ATATATAT others(21): Show |
A | 5 | a0001c0001t0003g0175a0001c0001t0003g0176a0001c0001t0011g0173others(2): Show | 5 | HG00280.hp2 HG04184.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6841_77+6868del others(28): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938063 | ||||||
chr5:60938065
|
ATATATAT others(19): Show |
A | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(55): Show | 62 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.77+6841_77+6866del others(26): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938065 | ||||||
chr5:60938065
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0003g0043 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.77+6840_77+6866del others(27): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938065 | ||||||
chr5:60938067
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+6844_77+6864del others(21): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938067 | ||||||
chr5:60938067
|
ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0158a0001c0001t0011g0157 | 2 | HG01346.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.77+6840_77+6864del others(25): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938067 | ||||||
chr5:60938067
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0003g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.77+6839_77+6864del others(26): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938067 | ||||||
chr5:60938068
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+6842_77+6863del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938068 | ||||||
chr5:60938069
|
ATATATAT others(15): Show |
A | 4 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(1): Show | 4 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+6841_77+6862del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938069 | ||||||
chr5:60938070
|
TATATATA others(13): Show |
T | 15 | a0001c0002t0008g0046a0001c0002t0008g0047a0001c0002t0008g0073others(12): Show | 15 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+6842_77+6861del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938070 | ||||||
chr5:60938072
|
TATATATA others(11): Show |
T | 9 | a0001c0002t0006g0049a0001c0002t0006g0060a0001c0002t0006g0061others(6): Show | 9 | HG00280.hp1 HG01496.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+6842_77+6859del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938072 | ||||||
chr5:60938073
|
ATATATAT others(11): Show |
A | 2 | a0001c0002t0006g0084a0001c0002t0016g0082 | 2 | HG02809.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.77+6841_77+6858del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938073 | ||||||
chr5:60938073
|
ATATATAT others(13): Show |
A | 1 | a0001c0009t0034g0020 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.77+6839_77+6858del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938073 | ||||||
chr5:60938074
|
TATATATA others(9): Show |
T | 9 | a0001c0001t0018g0066a0001c0002t0006g0056a0001c0002t0006g0057others(6): Show | 9 | HG00642.hp1 HG01192.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+6842_77+6857del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938074 | ||||||
chr5:60938075
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+6841_77+6856del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938075 | ||||||
chr5:60938080
|
TATATA | T | 3 | a0001c0001t0023g0284a0001c0001t0023g0285a0001c0003t0024g0008 | 3 | HG01109.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.77+6847_77+6851del others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938080 | ||||||
chr5:60938082
|
TATATTTT others(1): Show |
T | 3 | a0001c0001t0002g0219a0001c0001t0009g0189a0001c0001t0079g0218 | 3 | HG00733.hp1 NA18945.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.77+6842_77+6849del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938082 | ||||||
chr5:60938084
|
TATTTTA | T | 3 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0217 | 3 | NA19065.hp1 NA19086.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.77+6842_77+6847del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938084 | ||||||
chr5:60938085
|
A | T | 1 | a0001c0001t0007g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.77+6847T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938085 | ||||||
chr5:60938085
|
ATTT | A | 5 | a0001c0001t0002g0231a0001c0001t0003g0170a0001c0001t0020g0108others(2): Show | 5 | HG03927.hp1 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+6844_77+6846del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938085 | ||||||
chr5:60938085
|
ATTTTAT | A | 21 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0115others(18): Show | 21 | HG00621.hp1 HG00639.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.77+6841_77+6846del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938085 | ||||||
chr5:60938086
|
TTTTA | T | 35 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0002g0005others(32): Show | 36 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.77+6842_77+6845del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938086 | ||||||
chr5:60938087
|
T | A | 5 | a0001c0001t0002g0199a0001c0001t0002g0212a0001c0001t0002g0294others(2): Show | 5 | HG00621.hp2 HG01074.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6845A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938087 | ||||||
chr5:60938087
|
TTTA | T | 12 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0198others(9): Show | 12 | HG00738.hp2 HG01255.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.77+6842_77+6844del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938087 | ||||||
chr5:60938088
|
TTA | T | 22 | a0001c0001t0002g0199a0001c0001t0002g0208a0001c0001t0002g0209others(19): Show | 23 | HG00621.hp2 HG01074.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+6842_77+6843del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938088 | ||||||
chr5:60938089
|
T | A | 1 | a0001c0001t0023g0289 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.77+6843A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938089 | ||||||
chr5:60938089
|
TA | T | 18 | a0001c0001t0002g0294a0001c0001t0007g0015a0001c0001t0007g0016others(15): Show | 18 | HG01361.hp1 HG01884.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+6842delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938089 | ||||||
chr5:60938090
|
A | G | 1 | a0001c0001t0005g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.77+6842T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938090 | ||||||
chr5:60938090
|
A | T | 20 | a0001c0001t0007g0025a0001c0001t0010g0002a0001c0001t0010g0026others(17): Show | 21 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+6842T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938090 | ||||||
chr5:60938095
|
T | A | 1 | a0001c0001t0047g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77+6837A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938095 | ||||||
chr5:60938339
|
T | C | 18 | a0001c0001t0001g0166a0001c0001t0003g0041a0001c0001t0003g0042others(15): Show | 18 | HG00280.hp2 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+6593A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938339 | ||||||
chr5:60938348
|
GA | G | 52 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0002g0198others(49): Show | 53 | HG00140.hp2 HG00673.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.77+6583delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938348 | ||||||
chr5:60938349
|
AAT | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(116): Show | 125 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.77+6581_77+6582del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938349 | ||||||
chr5:60938349
|
AATT | A | 20 | a0001c0001t0001g0166a0001c0001t0003g0041a0001c0001t0003g0042others(17): Show | 20 | HG00280.hp2 HG00558.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.77+6580_77+6582del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938349 | ||||||
chr5:60938350
|
A | AT | 25 | a0001c0001t0005g0268a0001c0001t0015g0259a0001c0001t0018g0247others(22): Show | 25 | HG00280.hp1 HG00642.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+6581dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938350 | ||||||
chr5:60938350
|
A | T | 9 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0195others(6): Show | 9 | HG01981.hp2 HG02257.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+6582T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938350 | ||||||
chr5:60938377
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+6555G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938377 | ||||||
chr5:60938394
|
G | A | 1 | a0001c0001t0041g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.77+6538C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938394 | ||||||
chr5:60938415
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(117): Show | 125 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.77+6517T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938415 | ||||||
chr5:60938502
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+6430A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938502 | ||||||
chr5:60938512
|
C | G | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.77+6420G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938512 | ||||||
chr5:60938513
|
C | A | 1 | a0001c0003t0024g0007 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+6419G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938513 | ||||||
chr5:60938514
|
C | A | 1 | a0001c0003t0024g0007 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+6418G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938514 | ||||||
chr5:60938542
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.77+6390G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938542 | ||||||
chr5:60938588
|
A | G | 1 | a0001c0003t0024g0007 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+6344T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938588 | ||||||
chr5:60938602
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(245): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.77+6330A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938602 | ||||||
chr5:60938634
|
G | T | 2 | a0001c0001t0012g0185a0001c0001t0012g0186 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.77+6298C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938634 | ||||||
chr5:60938644
|
G | T | 1 | a0001c0001t0004g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.77+6288C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938644 | ||||||
chr5:60938762
|
A | T | 1 | a0001c0001t0005g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77+6170T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938762 | ||||||
chr5:60938876
|
G | A | 1 | a0001c0004t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.77+6056C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938876 | ||||||
chr5:60938909
|
G | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+6023C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938909 | ||||||
chr5:60939005
|
G | T | 14 | a0001c0002t0006g0049a0001c0002t0006g0056a0001c0002t0006g0057others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+5927C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939005 | ||||||
chr5:60939076
|
G | C | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+5856C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939076 | ||||||
chr5:60939327
|
G | A | 1 | a0001c0004t0039g0161 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.77+5605C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939327 | ||||||
chr5:60939362
|
G | A | 2 | a0001c0001t0012g0185a0001c0001t0012g0186 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.77+5570C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939362 | ||||||
chr5:60939413
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(204): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.77+5519C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939413 | ||||||
chr5:60939478
|
CTTT | C | 38 | a0001c0001t0018g0066a0001c0002t0006g0049a0001c0002t0006g0056others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.77+5451_77+5453del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939478 | ||||||
chr5:60939487
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(203): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.77+5445T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939487 | ||||||
chr5:60939554
|
G | C | 3 | a0001c0002t0006g0049a0001c0002t0006g0083a0001c0002t0006g0084 | 3 | HG03490.hp1 HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.77+5378C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939554 | ||||||
chr5:60939639
|
C | T | 1 | a0001c0001t0075g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.77+5293G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939639 | ||||||
chr5:60939645
|
C | T | 6 | a0001c0003t0024g0007a0001c0003t0024g0008a0001c0003t0025g0009others(3): Show | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+5287G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939645 | ||||||
chr5:60939656
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(105): Show | 113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.77+5276G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939656 | ||||||
chr5:60939762
|
C | T | 7 | a0001c0001t0022g0286a0001c0001t0022g0288a0001c0001t0022g0290others(4): Show | 7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+5170G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939762 | ||||||
chr5:60940109
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.77+4823A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940109 | ||||||
chr5:60940207
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.77+4725T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940207 | ||||||
chr5:60940379
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(245): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.77+4553T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940379 | ||||||
chr5:60940512
|
A | T | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4420T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940512 | ||||||
chr5:60940513
|
G | T | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4419C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940513 | ||||||
chr5:60940514
|
A | C | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4418T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940514 | ||||||
chr5:60940515
|
A | T | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4417T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940515 | ||||||
chr5:60940522
|
A | C | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4410T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940522 | ||||||
chr5:60940606
|
T | C | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+4326A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940606 | ||||||
chr5:60940635
|
G | A | 5 | a0001c0001t0034g0051a0001c0001t0058g0262a0001c0001t0059g0263others(2): Show | 5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+4297C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940635 | ||||||
chr5:60940653
|
A | C | 12 | a0001c0001t0004g0006a0001c0001t0004g0237a0001c0001t0004g0238others(9): Show | 13 | HG02004.hp1 HG02132.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.77+4279T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940653 | ||||||
chr5:60940703
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.77+4229G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940703 | ||||||
chr5:60940848
|
G | A | 1 | a0001c0001t0044g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4084C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940848 | ||||||
chr5:60940909
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+4023C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940909 | ||||||
chr5:60941075
|
T | G | 1 | a0001c0005t0020g0004 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.77+3857A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941075 | ||||||
chr5:60941122
|
C | T | 1 | a0001c0001t0011g0093 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.77+3810G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941122 | ||||||
chr5:60941284
|
T | A | 2 | a0001c0001t0003g0164a0001c0001t0038g0163 | 2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.77+3648A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941284 | ||||||
chr5:60941325
|
G | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02523.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.77+3607C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941325 | ||||||
chr5:60941609
|
T | A | 1 | a0001c0001t0073g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.77+3323A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941609 | ||||||
chr5:60941792
|
A | C | 5 | a0001c0001t0014g0088a0001c0001t0014g0089a0001c0001t0014g0090others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+3140T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941792 | ||||||
chr5:60941869
|
G | T | 38 | a0001c0001t0018g0066a0001c0002t0006g0049a0001c0002t0006g0056others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.77+3063C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941869 | ||||||
chr5:60941944
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+2988T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941944 | ||||||
chr5:60941946
|
A | G | 1 | a0001c0001t0009g0292 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.77+2986T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941946 | ||||||
chr5:60942059
|
A | G | 2 | a0001c0001t0004g0237a0001c0001t0004g0238 | 2 | NA18612.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.77+2873T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942059 | ||||||
chr5:60942141
|
C | G | 1 | a0001c0002t0053g0055 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.77+2791G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942141 | ||||||
chr5:60942157
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+2775G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942157 | ||||||
chr5:60942299
|
T | C | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+2633A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942299 | ||||||
chr5:60942425
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+2507T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942425 | ||||||
chr5:60942680
|
A | C | 2 | a0001c0001t0029g0264a0001c0001t0029g0265 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77+2252T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942680 | ||||||
chr5:60942763
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(168): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+2169T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942763 | ||||||
chr5:60942831
|
G | A | 18 | a0001c0001t0001g0166a0001c0001t0003g0041a0001c0001t0003g0042others(15): Show | 18 | HG00280.hp2 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+2101C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942831 | ||||||
chr5:60942869
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+2063G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942869 | ||||||
chr5:60942908
|
A | T | 22 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0018others(19): Show | 23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.77+2024T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942908 | ||||||
chr5:60942934
|
A | G | 1 | a0001c0001t0009g0190 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.77+1998T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942934 | ||||||
chr5:60942979
|
A | T | 1 | a0001c0001t0009g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.77+1953T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942979 | ||||||
chr5:60943006
|
C | T | 4 | a0001c0001t0003g0050a0001c0001t0003g0085a0001c0001t0003g0086others(1): Show | 4 | NA18612.hp2 NA18945.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+1926G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943006 | ||||||
chr5:60943038
|
AG | A | 3 | a0001c0001t0028g0038a0001c0001t0028g0039a0001c0001t0044g0179 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+1893delC | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943038 | ||||||
chr5:60943067
|
T | C | 1 | a0001c0001t0007g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.77+1865A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943067 | ||||||
chr5:60943107
|
C | T | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+1825G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943107 | ||||||
chr5:60943616
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+1316C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943616 | ||||||
chr5:60943734
|
G | A | 1 | a0001c0001t0076g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+1198C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943734 | ||||||
chr5:60943871
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(197): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+1061G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943871 | ||||||
chr5:60943973
|
G | A | 7 | a0001c0001t0043g0013a0001c0003t0024g0007a0001c0003t0024g0008others(4): Show | 7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+959C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943973 | ||||||
chr5:60944016
|
C | T | 3 | a0001c0001t0015g0259a0001c0001t0015g0260a0001c0001t0015g0261 | 3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.77+916G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944016 | ||||||
chr5:60944135
|
ATC | A | 7 | a0001c0001t0012g0181a0001c0001t0012g0182a0001c0001t0012g0183others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+795_77+796delGA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944135 | ||||||
chr5:60944216
|
T | C | 1 | a0001c0001t0042g0037 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.77+716A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944216 | ||||||
chr5:60944337
|
G | A | 1 | a0001c0004t0078g0187 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.77+595C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944337 | ||||||
chr5:60944641
|
G | T | 1 | a0001c0001t0009g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.77+291C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944641 | ||||||
chr5:60944705
|
A | AC | 33 | a0001c0001t0001g0040a0001c0001t0003g0041a0001c0001t0003g0042others(30): Show | 34 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.77+226dupG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944705 | ||||||
chr5:60944705
|
AC | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0094others(119): Show | 127 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.77+226delG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944705 | ||||||
chr5:60944705
|
ACC | A | 70 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0193others(67): Show | 72 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.77+225_77+226delGG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944705 | ||||||
chr5:60944706
|
CCCCCCCC others(14): Show |
C | 2 | a0001c0001t0028g0038a0001c0001t0028g0039 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+205_77+225delTT others(19): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944706 | ||||||
chr5:60944727
|
A | AC | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0040others(198): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+204dupG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944727 | ||||||
chr5:60944727
|
A | ACC | 27 | a0001c0001t0002g0036a0001c0001t0002g0294a0001c0001t0007g0015others(24): Show | 28 | HG01099.hp2 HG01361.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.77+203_77+204dupGG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944727 | ||||||
chr5:60944916
|
G | A | 2 | a0001c0001t0002g0294a0001c0001t0009g0293 | 2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.77+16C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944916 |