Item | Value |
---|---|
geneid | 2073 |
ensemblid | ENSG00000134899.24 |
hgncid | 3437 |
symbol | ERCC5 |
name | ERCC excision repair 5, endonuclease |
refseq_nuc | NM_000123.4 |
refseq_prot | NP_000114.3 |
ensembl_nuc | ENST00000652225.2 |
ensembl_prot | ENSP00000498881.2 |
mane_status | MANE Select |
chr | chr13 |
start | 102846032 |
end | 102875995 |
strand | + |
ver | v1.2 |
region | chr13:102846032-102875995 |
region5000 | chr13:102841032-102880995 |
regionname0 | ERCC5_chr13_102846032_102875995 |
regionname5000 | ERCC5_chr13_102841032_102880995 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1186 | 187 | 29 | 41 | 86 | 8 | 23 | 66 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0002 | 0/0 | 1186 | 138 | 41 | 15 | 69 | 6 | 7 | 56 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0003 | 0/0 | 1186 | 17 | 4 | 1 | 8 | 0 | 4 | 7 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0004 | 0/0 | 1186 | 13 | 8 | 4 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0005 | 0/0 | 1186 | 7 | 0 | 2 | 0 | 1 | 4 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0006 | 0/0 | 1186 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0007 | 0/0 | 1186 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0008 | 0/0 | 1186 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0009 | 0/0 | 1186 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0010 | 0/0 | 1186 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0011 | 0/0 | 1186 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0012 | 0/0 | 1186 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0013 | 0/0 | 1186 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0014 | 0/0 | 1186 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0015 | 0/0 | 1186 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0016 | 0/0 | 1186 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0017 | 0/0 | 1186 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0018 | 0/0 | 1186 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0019 | 0/0 | 1186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0020 | 0/0 | 1186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0021 | 0/0 | 1186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(1181): Show |
chr13 | 102841032 | 102880995 |
a0022 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(899): Show |
chr13 | 102841032 | 102880995 |
a0023 | 0/0 | 39 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | MGVQG others(34): Show |
chr13 | 102841032 | 102880995 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3558 | 99 | 16 | 21 | 52 | 0 | 10 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0001c0003 | 0/0 | 3558 | 76 | 13 | 19 | 23 | 8 | 13 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0001c0008 | 0/0 | 3558 | 9 | 0 | 0 | 9 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0001c0025 | 0/0 | 3558 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0001c0033 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0001c0037 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0002c0002 | 0/0 | 3558 | 96 | 10 | 11 | 64 | 5 | 6 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0002c0004 | 0/0 | 3558 | 20 | 14 | 2 | 3 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0002c0005 | 0/0 | 3558 | 18 | 17 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0002c0017 | 0/0 | 3558 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0002c0027 | 0/0 | 3558 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0002c0029 | 0/0 | 3558 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0003c0006 | 0/0 | 3558 | 16 | 3 | 1 | 8 | 0 | 4 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0003c0022 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0004c0007 | 0/0 | 3558 | 11 | 7 | 4 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0004c0018 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0004c0035 | 0/0 | 3558 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0005c0009 | 0/0 | 3558 | 7 | 0 | 2 | 0 | 1 | 4 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0006c0011 | 0/0 | 3558 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0007c0010 | 0/0 | 3558 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0008c0013 | 0/0 | 3558 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0008c0019 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0009c0012 | 0/0 | 3558 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0010c0015 | 0/0 | 3558 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0011c0016 | 0/0 | 3558 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0012c0014 | 0/0 | 3558 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0013c0024 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0014c0034 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0015c0032 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0016c0023 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0017c0028 | 0/0 | 3558 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0018c0020 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0019c0021 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0020c0031 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0021c0026 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0022c0030 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3553): Show |
chr13 | 102841032 | 102880995 | ||
a0023c0036 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | ATGGG others(3559): Show |
chr13 | 102841032 | 102880995 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3888 | 92 | 10 | 21 | 51 | 0 | 10 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0001t0002 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0001t0005 | 0/0 | 3888 | 5 | 4 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0001t0008 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0003t0001 | 0/0 | 3888 | 63 | 7 | 15 | 23 | 5 | 13 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0003t0002 | 0/0 | 3888 | 8 | 1 | 4 | 0 | 3 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0003t0003 | 0/0 | 3888 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0003t0010 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0008t0001 | 0/0 | 3888 | 7 | 0 | 0 | 7 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0008t0002 | 0/0 | 3888 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0025t0001 | 0/0 | 3888 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0033t0001 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0001c0037t0001 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0002t0001 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0002t0002 | 0/0 | 3888 | 94 | 10 | 11 | 62 | 5 | 6 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0002t0005 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0004t0002 | 0/0 | 3888 | 19 | 13 | 2 | 3 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0004t0009 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0005t0002 | 0/0 | 3888 | 18 | 17 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0017t0002 | 0/0 | 3888 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0027t0002 | 0/0 | 3888 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0002c0029t0002 | 0/0 | 3888 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0003c0006t0003 | 0/0 | 3888 | 11 | 3 | 0 | 8 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0003c0006t0006 | 0/0 | 3888 | 4 | 0 | 1 | 0 | 0 | 3 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0003c0006t0007 | 0/0 | 3888 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0003c0022t0003 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0004c0007t0002 | 0/0 | 3888 | 5 | 4 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0004c0007t0004 | 0/0 | 3888 | 6 | 3 | 3 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0004c0018t0004 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0004c0035t0001 | 0/0 | 3888 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0005c0009t0001 | 0/0 | 3888 | 7 | 0 | 2 | 0 | 1 | 4 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0006c0011t0002 | 0/0 | 3888 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0007c0010t0002 | 0/0 | 3888 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0008c0013t0002 | 0/0 | 3888 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0008c0019t0002 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0009c0012t0002 | 0/0 | 3888 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0010c0015t0001 | 0/0 | 3888 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0011c0016t0002 | 0/0 | 3888 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0012c0014t0002 | 0/0 | 3888 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0013c0024t0004 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0014c0034t0002 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0015c0032t0001 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0016c0023t0003 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0017c0028t0002 | 0/0 | 3888 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0018c0020t0002 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0019c0021t0001 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0020c0031t0001 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0021c0026t0002 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0022c0030t0002 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3883): Show |
chr13 | 102841032 | 102880995 |
a0023c0036t0002 | 0/0 | 3894 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | CTTCC others(3889): Show |
chr13 | 102841032 | 102880995 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 10 | 1 | 1 | 3 | 0 | 5 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0017 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0001 | 0/0 | 12 | 0 | 1 | 8 | 0 | 3 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0006 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0014 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0015 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0003t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0008t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0025t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0033t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0001c0037t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0004 | 0/0 | 7 | 1 | 0 | 3 | 2 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0027 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0004t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0003 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0005t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0017t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0017t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0027t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0002c0029t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0016 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0006t0007g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0003c0022t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0004g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0007t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0018t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0004c0035t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0005c0009t0001g0001 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0005c0009t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0005c0009t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0006c0011t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0007c0010t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0007c0010t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0008c0013t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0008c0019t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0009c0012t0002g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0010c0015t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0010c0015t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0011c0016t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0012c0014t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0013c0024t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0014c0034t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0015c0032t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0016c0023t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0017c0028t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0018c0020t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0019c0021t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0020c0031t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0021c0026t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0022c0030t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
a0023c0036t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0033 | EUR | GBR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00099 | hp2 | a0010 | c0015 | t0001 | g0021 | EUR | GBR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0178 | EUR | GBR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | GBR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0020 | EUR | FIN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00280 | hp2 | a0001 | c0003 | t0002 | g0067 | EUR | FIN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0068 | EUR | FIN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0007 | EUR | FIN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00639 | hp2 | a0004 | c0007 | t0004 | g0029 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | CHS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00733 | hp1 | a0001 | c0025 | t0001 | g0198 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00741 | hp1 | a0004 | c0007 | t0004 | g0029 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01069 | hp2 | a0003 | c0006 | t0006 | g0098 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0088 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0078 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01099 | hp1 | a0005 | c0009 | t0001 | g0001 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01109 | hp1 | a0002 | c0004 | t0002 | g0093 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01167 | hp1 | a0002 | c0029 | t0002 | g0161 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01168 | hp2 | a0004 | c0007 | t0004 | g0029 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01169 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01192 | hp1 | a0002 | c0004 | t0002 | g0113 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01192 | hp2 | a0010 | c0015 | t0001 | g0079 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01243 | hp1 | a0004 | c0007 | t0002 | g0045 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0182 | AMR | PUR | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01358 | hp2 | a0005 | c0009 | t0001 | g0001 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0007 | AMR | CLM | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0027 | EUR | IBS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01884 | hp1 | a0004 | c0007 | t0002 | g0010 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01884 | hp2 | a0008 | c0013 | t0002 | g0023 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0184 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01891 | hp2 | a0004 | c0007 | t0004 | g0010 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0020 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0153 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01975 | hp1 | a0002 | c0005 | t0002 | g0024 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0080 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01978 | hp2 | a0011 | c0016 | t0002 | g0042 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0151 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0084 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02015 | hp2 | a0003 | c0006 | t0003 | g0106 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02055 | hp1 | a0013 | c0024 | t0004 | g0010 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02055 | hp2 | a0004 | c0007 | t0002 | g0045 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02071 | hp2 | a0002 | c0004 | t0002 | g0006 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02135 | hp1 | a0001 | c0008 | t0001 | g0031 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02135 | hp2 | a0009 | c0012 | t0002 | g0028 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02145 | hp1 | a0002 | c0005 | t0002 | g0003 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02148 | hp1 | a0011 | c0016 | t0002 | g0042 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02155 | hp1 | a0014 | c0034 | t0002 | g0149 | EAS | CDX | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | CDX | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0095 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02257 | hp2 | a0002 | c0004 | t0002 | g0089 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02258 | hp2 | a0003 | c0006 | t0003 | g0016 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02280 | hp1 | a0002 | c0004 | t0002 | g0116 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0179 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0174 | AMR | PEL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02451 | hp1 | a0001 | c0003 | t0003 | g0055 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02451 | hp2 | a0002 | c0005 | t0002 | g0123 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | KHV | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02572 | hp2 | a0004 | c0018 | t0004 | g0010 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02615 | hp1 | a0006 | c0011 | t0002 | g0018 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02615 | hp2 | a0002 | c0005 | t0002 | g0003 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02622 | hp1 | a0015 | c0032 | t0001 | g0223 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02622 | hp2 | a0002 | c0004 | t0002 | g0117 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02630 | hp1 | a0002 | c0005 | t0002 | g0003 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02630 | hp2 | a0007 | c0010 | t0002 | g0019 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02647 | hp1 | a0016 | c0023 | t0003 | g0247 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02723 | hp1 | a0002 | c0005 | t0002 | g0003 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02735 | hp2 | a0002 | c0004 | t0002 | g0063 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0090 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0158 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02818 | hp1 | a0002 | c0005 | t0002 | g0121 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02886 | hp1 | a0007 | c0010 | t0002 | g0062 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02886 | hp2 | a0002 | c0005 | t0002 | g0003 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0162 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02896 | hp1 | a0012 | c0014 | t0002 | g0008 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02897 | hp2 | a0012 | c0014 | t0002 | g0008 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02922 | hp1 | a0002 | c0005 | t0002 | g0024 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02922 | hp2 | a0002 | c0004 | t0002 | g0008 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02970 | hp1 | a0002 | c0005 | t0002 | g0024 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02970 | hp2 | a0004 | c0007 | t0004 | g0010 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02976 | hp1 | a0006 | c0011 | t0002 | g0018 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03041 | hp1 | a0004 | c0007 | t0002 | g0192 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03041 | hp2 | a0002 | c0005 | t0002 | g0003 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03098 | hp1 | a0008 | c0013 | t0002 | g0023 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03098 | hp2 | a0007 | c0010 | t0002 | g0019 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03130 | hp1 | a0003 | c0006 | t0003 | g0105 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03139 | hp1 | a0002 | c0004 | t0002 | g0008 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03139 | hp2 | a0002 | c0005 | t0002 | g0003 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03195 | hp1 | a0001 | c0003 | t0003 | g0248 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03195 | hp2 | a0002 | c0005 | t0002 | g0120 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0091 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03209 | hp2 | a0001 | c0003 | t0003 | g0055 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03225 | hp2 | a0002 | c0004 | t0002 | g0118 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0185 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03453 | hp2 | a0007 | c0010 | t0002 | g0019 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03486 | hp1 | a0002 | c0004 | t0002 | g0124 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03486 | hp2 | a0002 | c0004 | t0002 | g0074 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03516 | hp2 | a0002 | c0005 | t0002 | g0115 | AFR | ESN | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03540 | hp1 | a0006 | c0011 | t0002 | g0018 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0064 | AFR | GWD | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0092 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0071 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03654 | hp2 | a0003 | c0006 | t0006 | g0100 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0148 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | PJL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03831 | hp2 | a0005 | c0009 | t0001 | g0070 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03834 | hp2 | a0003 | c0006 | t0007 | g0099 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0180 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04115 | hp2 | a0004 | c0035 | t0001 | g0002 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04184 | hp1 | a0005 | c0009 | t0001 | g0001 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04184 | hp2 | a0003 | c0006 | t0006 | g0101 | SAS | BEB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04199 | hp1 | a0005 | c0009 | t0001 | g0085 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04204 | hp1 | a0003 | c0006 | t0006 | g0102 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG04228 | hp2 | a0017 | c0028 | t0002 | g0041 | SAS | STU | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18522 | hp1 | a0001 | c0003 | t0010 | g0057 | AFR | YRI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18522 | hp2 | a0002 | c0004 | t0009 | g0008 | AFR | YRI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | YRI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18906 | hp2 | a0002 | c0005 | t0002 | g0122 | AFR | YRI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18939 | hp2 | a0003 | c0006 | t0003 | g0016 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18940 | hp1 | a0002 | c0004 | t0002 | g0082 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18942 | hp2 | a0001 | c0037 | t0001 | g0217 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18944 | hp2 | a0003 | c0006 | t0003 | g0107 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18945 | hp1 | a0001 | c0033 | t0001 | g0238 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0096 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18947 | hp1 | a0002 | c0002 | t0005 | g0236 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18948 | hp1 | a0001 | c0008 | t0001 | g0228 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18966 | hp2 | a0002 | c0017 | t0002 | g0009 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18968 | hp2 | a0002 | c0017 | t0002 | g0175 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18972 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18974 | hp1 | a0019 | c0021 | t0001 | g0104 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18977 | hp2 | a0002 | c0004 | t0002 | g0066 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18981 | hp2 | a0020 | c0031 | t0001 | g0051 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18988 | hp2 | a0021 | c0026 | t0002 | g0164 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18989 | hp1 | a0003 | c0006 | t0003 | g0016 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18992 | hp1 | a0003 | c0006 | t0003 | g0034 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18992 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18995 | hp1 | a0001 | c0008 | t0002 | g0049 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18998 | hp1 | a0001 | c0008 | t0001 | g0208 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA18999 | hp2 | a0001 | c0008 | t0001 | g0051 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19003 | hp2 | a0001 | c0008 | t0001 | g0201 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19009 | hp2 | a0001 | c0008 | t0001 | g0050 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19011 | hp2 | a0001 | c0008 | t0002 | g0049 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19030 | hp1 | a0002 | c0004 | t0002 | g0119 | AFR | LWK | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19030 | hp2 | a0003 | c0022 | t0003 | g0097 | AFR | LWK | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19043 | hp1 | a0002 | c0004 | t0002 | g0112 | AFR | LWK | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19043 | hp2 | a0002 | c0004 | t0002 | g0035 | AFR | LWK | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19058 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19059 | hp1 | a0022 | c0030 | t0002 | g0061 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19059 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19060 | hp2 | a0003 | c0006 | t0003 | g0034 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19062 | hp2 | a0009 | c0012 | t0002 | g0028 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19065 | hp2 | a0003 | c0006 | t0003 | g0103 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19067 | hp1 | a0009 | c0012 | t0002 | g0028 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19068 | hp1 | a0001 | c0008 | t0001 | g0050 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19074 | hp1 | a0003 | c0006 | t0003 | g0108 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19075 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19076 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19076 | hp2 | a0023 | c0036 | t0002 | g0125 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA19240 | hp2 | a0008 | c0019 | t0002 | g0023 | AFR | YRI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20129 | hp2 | a0004 | c0007 | t0002 | g0191 | AFR | ASW | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20752 | hp1 | a0002 | c0027 | t0002 | g0025 | EUR | TSI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0027 | EUR | TSI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20805 | hp1 | a0005 | c0009 | t0001 | g0001 | EUR | TSI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0094 | EUR | TSI | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20905 | hp1 | a0005 | c0009 | t0001 | g0001 | SAS | GIH | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | GIH | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02109 | hp1 | a0002 | c0005 | t0002 | g0003 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02486 | hp1 | a0002 | c0005 | t0002 | g0003 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02486 | hp2 | a0002 | c0004 | t0002 | g0035 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG02559 | hp2 | a0003 | c0006 | t0003 | g0016 | AFR | ACB | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03471 | hp1 | a0004 | c0007 | t0004 | g0193 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG03471 | hp2 | a0002 | c0005 | t0002 | g0003 | AFR | MSL | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG06807 | hp1 | a0018 | c0020 | t0002 | g0246 | AFR | USA | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | USA | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA20300 | hp2 | a0002 | c0004 | t0002 | g0250 | AFR | USA | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | LWK | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | LWK | ERCC5_chr13_102841032_102880995 | ERCC5 | chr13 | 102841032 | 102880995 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102852144 | C | CT | 1 | a0023 | 1 | NA19076.hp2 | frameshift_variant&stop_gained | HIGH | c.117dupT | p.Lys40fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/15 | 353/3888 | 118/3561 | 40/1186 | INFO_REALIGN_3_PRIME | chr13 | 102852144 | ||
chr13:102852243 | C | CT | 1 | a0023 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.214_215insT | p.Pro72fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/15 | 450/3888 | 215/3561 | 72/1186 | chr13 | 102852243 | |||
chr13:102853763 | A | AG | 1 | a0023 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.272dupG | p.Arg92fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/15 | 508/3888 | 273/3561 | 91/1186 | INFO_REALIGN_3_PRIME | chr13 | 102853763 | ||
chr13:102853779 | A | ACT | 1 | a0023 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.288_289dupCT | p.Leu97fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/15 | 525/3888 | 290/3561 | 97/1186 | INFO_REALIGN_3_PRIME | chr13 | 102853779 | ||
chr13:102853799 | A | AG | 1 | a0023 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.309dupG | p.Lys104fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/15 | 545/3888 | 310/3561 | 104/1186 | INFO_REALIGN_3_PRIME | chr13 | 102853799 | ||
chr13:102854340 | G | A | 1 | a0008 | 3 | HG01884.hp2 HG03098.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.433G>A | p.Val145Ile | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/15 | 668/3888 | 433/3561 | 145/1186 | chr13 | 102854340 | |||
chr13:102858386 | C | T | 1 | a0009 | 3 | HG02135.hp2 NA19062.hp2 NA19067.hp1 |
missense_variant | MODERATE | c.640C>T | p.Arg214Cys | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/15 | 875/3888 | 640/3561 | 214/1186 | chr13 | 102858386 | |||
chr13:102858387 | G | A | 1 | a0007 | 4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.641G>A | p.Arg214His | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/15 | 876/3888 | 641/3561 | 214/1186 | chr13 | 102858387 | |||
chr13:102858412 | G | A | 1 | a0018 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.666G>A | p.Met222Ile | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/15 | 901/3888 | 666/3561 | 222/1186 | chr13 | 102858412 | |||
chr13:102861594 | A | G | 1 | a0005 | 7 | HG01099.hp1 HG01358.hp2 HG03831.hp2 others(4): Show |
missense_variant | MODERATE | c.760A>G | p.Met254Val | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/15 | 995/3888 | 760/3561 | 254/1186 | chr13 | 102861594 | |||
chr13:102861601 | A | G | 3 | a0004 a0009 a0013 |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
missense_variant | MODERATE | c.767A>G | p.Gln256Arg | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/15 | 1002/3888 | 767/3561 | 256/1186 | chr13 | 102861601 | |||
chr13:102861602 | G | T | 1 | a0004 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.768G>T | p.Gln256His | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/15 | 1003/3888 | 768/3561 | 256/1186 | chr13 | 102861602 | |||
chr13:102861712 | A | T | 1 | a0014 | 1 | HG02155.hp1 | missense_variant&splice_region_variant | MODERATE | c.878A>T | p.Lys293Ile | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/15 | 1113/3888 | 878/3561 | 293/1186 | chr13 | 102861712 | |||
chr13:102862735 | G | C | 2 | a0003 a0019 |
18 | HG01069.hp2 HG02015.hp2 HG02258.hp2 others(15): Show |
missense_variant | MODERATE | c.1586G>C | p.Cys529Ser | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1821/3888 | 1586/3561 | 529/1186 | chr13 | 102862735 | |||
chr13:102862860 | C | T | 1 | a0015 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1711C>T | p.Pro571Ser | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1946/3888 | 1711/3561 | 571/1186 | chr13 | 102862860 | |||
chr13:102862951 | A | G | 1 | a0012 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1802A>G | p.Glu601Gly | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 2037/3888 | 1802/3561 | 601/1186 | chr13 | 102862951 | |||
chr13:102863029 | C | A | 1 | a0011 | 2 | HG01978.hp2 HG02148.hp1 |
missense_variant | MODERATE | c.1880C>A | p.Ala627Glu | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 2115/3888 | 1880/3561 | 627/1186 | chr13 | 102863029 | |||
chr13:102863083 | C | T | 1 | a0020 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1934C>T | p.Ser645Leu | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 2169/3888 | 1934/3561 | 645/1186 | chr13 | 102863083 | |||
chr13:102868215 | A | G | 1 | a0010 | 2 | HG00099.hp2 HG01192.hp2 |
missense_variant | MODERATE | c.2636A>G | p.Asn879Ser | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/15 | 2871/3888 | 2636/3561 | 879/1186 | chr13 | 102868215 | |||
chr13:102872217 | CA | C | 1 | a0022 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.2705delA | p.Asn902fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/15 | 2940/3888 | 2705/3561 | 902/1186 | INFO_REALIGN_3_PRIME | chr13 | 102872217 | ||
chr13:102872396 | A | C | 1 | a0016 | 1 | HG02647.hp1 | missense_variant&splice_region_variant | MODERATE | c.2877A>C | p.Arg959Ser | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/15 | 3112/3888 | 2877/3561 | 959/1186 | chr13 | 102872396 | |||
chr13:102875499 | G | C | 22 | a0001 a0002 a0003 others(19): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
missense_variant | MODERATE | c.3157G>C | p.Gly1053Arg | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3392/3888 | 3157/3561 | 1053/1186 | chr13 | 102875499 | |||
chr13:102875580 | G | C | 22 | a0001 a0002 a0003 others(19): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
missense_variant | MODERATE | c.3238G>C | p.Gly1080Arg | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3473/3888 | 3238/3561 | 1080/1186 | chr13 | 102875580 | |||
chr13:102875652 | G | C | 10 | a0002 a0003 a0008 others(7): Show |
167 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(164): Show |
missense_variant | MODERATE | c.3310G>C | p.Asp1104His | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3545/3888 | 3310/3561 | 1104/1186 | chr13 | 102875652 | |||
chr13:102875677 | A | ATG | 1 | a0022 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.3337_3338dupGT | p.Gln1114fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3574/3888 | 3339/3561 | 1113/1186 | INFO_REALIGN_3_PRIME | chr13 | 102875677 | ||
chr13:102875698 | C | T | 1 | a0017 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.3356C>T | p.Ala1119Val | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3591/3888 | 3356/3561 | 1119/1186 | chr13 | 102875698 | |||
chr13:102875754 | G | A | 1 | a0021 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.3412G>A | p.Val1138Met | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3647/3888 | 3412/3561 | 1138/1186 | chr13 | 102875754 | |||
chr13:102875791 | A | G | 1 | a0013 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.3449A>G | p.Asp1150Gly | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3684/3888 | 3449/3561 | 1150/1186 | chr13 | 102875791 | |||
chr13:102875849 | TG | T | 1 | a0022 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.3510delG | p.Lys1171fs | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3745/3888 | 3510/3561 | 1170/1186 | INFO_REALIGN_3_PRIME | chr13 | 102875849 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102846320 | C | T | 1 | a0001c0037 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.54C>T | p.Ser18Ser | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/15 | 289/3888 | 54/3561 | 18/1186 | chr13 | 102846320 | |||
chr13:102852167 | T | C | 18 | a0001c0003 a0002c0004 a0002c0005 others(15): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
synonymous_variant | LOW | c.138T>C | p.His46His | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/15 | 373/3888 | 138/3561 | 46/1186 | chr13 | 102852167 | |||
chr13:102852200 | T | G | 1 | a0004c0018 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.171T>G | p.Thr57Thr | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/15 | 406/3888 | 171/3561 | 57/1186 | chr13 | 102852200 | |||
chr13:102854336 | C | G | 4 | a0004c0007 a0004c0018 a0009c0012 others(1): Show |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
synonymous_variant | LOW | c.429C>G | p.Leu143Leu | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/15 | 664/3888 | 429/3561 | 143/1186 | chr13 | 102854336 | |||
chr13:102862109 | C | T | 1 | a0010c0015 | 2 | HG00099.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.960C>T | p.Asp320Asp | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1195/3888 | 960/3561 | 320/1186 | chr13 | 102862109 | |||
chr13:102862286 | C | T | 1 | a0002c0017 | 2 | NA18966.hp2 NA18968.hp2 |
synonymous_variant | LOW | c.1137C>T | p.Asp379Asp | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1372/3888 | 1137/3561 | 379/1186 | chr13 | 102862286 | |||
chr13:102862436 | T | C | 1 | a0001c0025 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.1287T>C | p.Asp429Asp | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1522/3888 | 1287/3561 | 429/1186 | chr13 | 102862436 | |||
chr13:102862520 | C | T | 1 | a0001c0033 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.1371C>T | p.His457His | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1606/3888 | 1371/3561 | 457/1186 | chr13 | 102862520 | |||
chr13:102862589 | C | T | 1 | a0002c0005 | 18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
synonymous_variant | LOW | c.1440C>T | p.His480His | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1675/3888 | 1440/3561 | 480/1186 | chr13 | 102862589 | |||
chr13:102862685 | C | T | 1 | a0018c0020 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1536C>T | p.Asp512Asp | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/15 | 1771/3888 | 1536/3561 | 512/1186 | chr13 | 102862685 | |||
chr13:102865686 | A | G | 1 | a0008c0019 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1974A>G | p.Gln658Gln | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 9/15 | 2209/3888 | 1974/3561 | 658/1186 | chr13 | 102865686 | |||
chr13:102865812 | C | A | 2 | a0001c0008 a0020c0031 |
10 | HG02135.hp1 NA18948.hp1 NA18981.hp2 others(7): Show |
synonymous_variant | LOW | c.2100C>A | p.Leu700Leu | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 9/15 | 2335/3888 | 2100/3561 | 700/1186 | chr13 | 102865812 | |||
chr13:102866769 | G | A | 2 | a0008c0013 a0008c0019 |
3 | HG01884.hp2 HG03098.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.2457G>A | p.Arg819Arg | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/15 | 2692/3888 | 2457/3561 | 819/1186 | chr13 | 102866769 | |||
chr13:102875519 | C | T | 1 | a0002c0029 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.3177C>T | p.Gly1059Gly | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3412/3888 | 3177/3561 | 1059/1186 | chr13 | 102875519 | |||
chr13:102875556 | A | C | 1 | a0003c0022 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3214A>C | p.Arg1072Arg | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3449/3888 | 3214/3561 | 1072/1186 | chr13 | 102875556 | |||
chr13:102875762 | T | C | 1 | a0002c0027 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.3420T>C | p.Asn1140Asn | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 3655/3888 | 3420/3561 | 1140/1186 | chr13 | 102875762 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102846049 | C | G | 1 | a0001c0003t0010 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/15 | 218 | chr13 | 102846049 | ||||||
chr13:102846193 | G | A | 3 | a0004c0007t0004 a0004c0018t0004 a0013c0024t0004 |
8 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-74G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/15 | 74 | chr13 | 102846193 | ||||||
chr13:102846195 | C | T | 7 | a0001c0001t0005 a0001c0003t0003 a0002c0002t0005 others(4): Show |
27 | HG01069.hp2 HG02015.hp2 HG02145.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-72C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/15 | 72 | chr13 | 102846195 | ||||||
chr13:102846204 | A | T | 1 | a0002c0004t0009 | 1 | NA18522.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/15 | chr13 | 102846204 | |||||||
chr13:102875960 | C | T | 1 | a0001c0001t0008 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 57 | chr13 | 102875960 | ||||||
chr13:102875987 | G | A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0003t0001 others(13): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*84G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 84 | chr13 | 102875987 | ||||||
chr13:102875992 | G | A | 2 | a0003c0006t0006 a0003c0006t0007 |
5 | HG01069.hp2 HG03654.hp2 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*89G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 15/15 | 89 | chr13 | 102875992 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102846527 | C | T | 1 | a0002c0004t0002g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.88+173C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102846527 | |||||||
chr13:102846556 | G | A | 5 | a0001c0003t0001g0056 a0001c0003t0001g0058 a0001c0003t0010g0057 others(2): Show |
5 | HG00558.hp2 HG00609.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+202G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102846556 | |||||||
chr13:102846666 | G | GCCGAATG others(4): Show |
1 | a0022c0030t0002g0061 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.88+313_88+323dupCC others(9): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102846666 | ||||||
chr13:102846697 | T | C | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+343T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102846697 | |||||||
chr13:102846717 | A | T | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+363A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102846717 | |||||||
chr13:102846742 | TTTTA | T | 5 | a0001c0001t0005g0249 a0001c0003t0003g0055 a0001c0003t0003g0248 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+400_88+403delAT others(2): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102846742 | ||||||
chr13:102846885 | G | A | 1 | a0002c0004t0002g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.88+531G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102846885 | |||||||
chr13:102846925 | T | C | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.88+571T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102846925 | |||||||
chr13:102847008 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.88+654T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847008 | |||||||
chr13:102847067 | C | A | 179 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0001g0110 others(176): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.88+713C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847067 | |||||||
chr13:102847104 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.88+750G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847104 | |||||||
chr13:102847141 | C | G | 104 | a0001c0001t0001g0026 a0001c0001t0001g0130 a0001c0001t0001g0131 others(101): Show |
140 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.88+787C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847141 | |||||||
chr13:102847188 | T | C | 1 | a0001c0003t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.88+834T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847188 | |||||||
chr13:102847290 | T | C | 71 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(68): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.88+936T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847290 | |||||||
chr13:102847297 | A | ATT | 13 | a0003c0006t0003g0034 a0003c0006t0003g0103 a0003c0006t0003g0105 others(10): Show |
14 | HG01069.hp2 HG02015.hp2 HG03130.hp1 others(11): Show |
intron_variant | MODIFIER | c.88+958_88+959dupTT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102847297 | ||||||
chr13:102847297 | AT | A | 45 | a0001c0001t0001g0190 a0001c0001t0008g0064 a0001c0003t0001g0001 others(42): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.88+959delT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102847297 | ||||||
chr13:102847350 | A | G | 66 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(63): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.88+996A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847350 | |||||||
chr13:102847365 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(17): Show |
35 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.88+1011A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847365 | |||||||
chr13:102847550 | T | C | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.88+1196T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847550 | |||||||
chr13:102847737 | C | G | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.88+1383C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847737 | |||||||
chr13:102847755 | T | C | 1 | a0003c0022t0003g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88+1401T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847755 | |||||||
chr13:102847831 | G | A | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+1477G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847831 | |||||||
chr13:102847886 | C | A | 5 | a0003c0006t0006g0098 a0003c0006t0006g0100 a0003c0006t0006g0101 others(2): Show |
5 | HG01069.hp2 HG03654.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+1532C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102847886 | |||||||
chr13:102848022 | G | T | 1 | a0001c0001t0001g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.88+1668G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848022 | |||||||
chr13:102848034 | C | G | 72 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(69): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.88+1680C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848034 | |||||||
chr13:102848039 | G | T | 2 | a0001c0003t0001g0086 a0001c0003t0001g0087 |
2 | NA18965.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.88+1685G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848039 | |||||||
chr13:102848108 | G | A | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.88+1754G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848108 | |||||||
chr13:102848165 | C | CATA | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.88+1813_88+1814ins others(3): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102848165 | ||||||
chr13:102848450 | G | T | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.88+2096G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848450 | |||||||
chr13:102848693 | C | T | 40 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0013 others(37): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.88+2339C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848693 | |||||||
chr13:102848716 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.88+2362G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848716 | |||||||
chr13:102848855 | C | G | 10 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(7): Show |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+2501C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848855 | |||||||
chr13:102848868 | T | C | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.88+2514T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848868 | |||||||
chr13:102848906 | T | A | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.88+2552T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848906 | |||||||
chr13:102848953 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.88+2599A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102848953 | |||||||
chr13:102849019 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.88+2665C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849019 | |||||||
chr13:102849088 | A | G | 1 | a0001c0003t0002g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.88+2734A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849088 | |||||||
chr13:102849197 | A | G | 1 | a0002c0002t0002g0054 | 2 | NA18959.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.88+2843A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849197 | |||||||
chr13:102849299 | C | A | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2819C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849299 | |||||||
chr13:102849353 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.89-2765G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849353 | |||||||
chr13:102849355 | A | C | 1 | a0002c0004t0002g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.89-2763A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849355 | |||||||
chr13:102849578 | CA | C | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-2539delA | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849578 | |||||||
chr13:102849579 | A | AT | 4 | a0002c0002t0002g0187 a0002c0002t0002g0188 a0007c0010t0002g0019 others(1): Show |
6 | HG02071.hp1 HG02523.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2530dupT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102849579 | ||||||
chr13:102849591 | G | A | 1 | a0002c0004t0002g0066 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.89-2527G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849591 | |||||||
chr13:102849638 | C | T | 1 | a0002c0002t0002g0186 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.89-2480C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849638 | |||||||
chr13:102849670 | T | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(73): Show |
113 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.89-2448T>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849670 | |||||||
chr13:102849693 | G | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0002c0002t0001g0233 |
3 | HG00408.hp2 HG00621.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.89-2425G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849693 | |||||||
chr13:102849854 | G | T | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-2264G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849854 | |||||||
chr13:102849884 | A | G | 2 | a0001c0003t0002g0091 a0001c0003t0003g0092 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89-2234A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849884 | |||||||
chr13:102849933 | G | GT | 8 | a0002c0002t0002g0059 a0002c0002t0002g0060 a0002c0002t0002g0181 others(5): Show |
8 | HG00558.hp2 HG00609.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-2175dupT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102849933 | ||||||
chr13:102849933 | GT | G | 37 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0056 others(34): Show |
50 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.89-2175delT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102849933 | ||||||
chr13:102849943 | T | TTC | 79 | a0001c0001t0001g0026 a0001c0001t0001g0130 a0001c0001t0001g0131 others(76): Show |
100 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.89-2175_89-2174ins others(2): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849943 | |||||||
chr13:102849982 | C | G | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-2136C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849982 | |||||||
chr13:102849990 | C | A | 2 | a0002c0002t0002g0181 a0002c0002t0002g0182 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.89-2128C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102849990 | |||||||
chr13:102850160 | A | G | 1 | a0007c0010t0002g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.89-1958A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850160 | |||||||
chr13:102850203 | A | T | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-1915A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850203 | |||||||
chr13:102850264 | T | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.89-1854T>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850264 | |||||||
chr13:102850289 | A | G | 6 | a0002c0002t0002g0027 a0002c0002t0002g0043 a0002c0002t0002g0044 others(3): Show |
10 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-1829A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850289 | |||||||
chr13:102850327 | C | T | 10 | a0002c0002t0002g0009 a0002c0002t0002g0114 a0002c0002t0002g0171 others(7): Show |
13 | HG00438.hp1 HG02040.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.89-1791C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850327 | |||||||
chr13:102850365 | C | T | 1 | a0002c0002t0002g0170 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.89-1753C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850365 | |||||||
chr13:102850449 | C | T | 2 | a0003c0006t0003g0107 a0003c0006t0003g0108 |
2 | NA18944.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.89-1669C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850449 | |||||||
chr13:102850493 | A | T | 20 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(17): Show |
35 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.89-1625A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850493 | |||||||
chr13:102850599 | T | C | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.89-1519T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850599 | |||||||
chr13:102850600 | G | T | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.89-1518G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850600 | |||||||
chr13:102850655 | C | G | 1 | a0001c0008t0001g0228 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.89-1463C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850655 | |||||||
chr13:102850656 | A | G | 1 | a0002c0004t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.89-1462A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850656 | |||||||
chr13:102850664 | A | T | 1 | a0002c0002t0002g0169 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.89-1454A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850664 | |||||||
chr13:102850672 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(160): Show |
221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.89-1446G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850672 | |||||||
chr13:102850811 | A | C | 1 | a0001c0003t0001g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.89-1307A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850811 | |||||||
chr13:102850972 | G | A | 67 | a0001c0001t0001g0194 a0001c0003t0001g0001 a0001c0003t0001g0006 others(64): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.89-1146G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102850972 | |||||||
chr13:102851002 | T | G | 1 | a0001c0003t0002g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.89-1116T>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851002 | |||||||
chr13:102851037 | A | G | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.89-1081A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851037 | |||||||
chr13:102851090 | A | C | 6 | a0001c0001t0001g0222 a0001c0001t0001g0224 a0001c0001t0001g0226 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1028A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851090 | |||||||
chr13:102851096 | A | T | 1 | a0001c0003t0003g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.89-1022A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851096 | |||||||
chr13:102851297 | A | ATTAGTTT others(3): Show |
1 | a0001c0001t0001g0109 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.89-818_89-809dupAG others(8): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102851297 | ||||||
chr13:102851319 | G | A | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-799G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851319 | |||||||
chr13:102851441 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(160): Show |
221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.89-677C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851441 | |||||||
chr13:102851514 | C | T | 10 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(7): Show |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-604C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851514 | |||||||
chr13:102851712 | G | A | 72 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(69): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.89-406G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851712 | |||||||
chr13:102851835 | A | AT | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.89-274dupT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 102851835 | ||||||
chr13:102851854 | A | G | 1 | a0002c0002t0002g0168 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.89-264A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851854 | |||||||
chr13:102851900 | G | A | 1 | a0002c0002t0002g0170 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.89-218G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851900 | |||||||
chr13:102851920 | G | A | 1 | a0002c0002t0002g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.89-198G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851920 | |||||||
chr13:102851963 | G | T | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.89-155G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851963 | |||||||
chr13:102851981 | T | C | 5 | a0002c0002t0002g0025 a0002c0002t0002g0126 a0002c0002t0002g0127 others(2): Show |
6 | HG00733.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-137T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851981 | |||||||
chr13:102851994 | A | G | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-124A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102851994 | |||||||
chr13:102852031 | G | C | 1 | a0002c0004t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.89-87G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 1/14 | chr13 | 102852031 | |||||||
chr13:102852300 | G | A | 20 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(17): Show |
35 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.264+7G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852300 | |||||||
chr13:102852410 | GAC | G | 9 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(6): Show |
21 | HG01884.hp2 HG01975.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.264+121_264+122del others(2): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 102852410 | ||||||
chr13:102852639 | G | A | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.264+346G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852639 | |||||||
chr13:102852813 | T | A | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.264+520T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852813 | |||||||
chr13:102852814 | A | T | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.264+521A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852814 | |||||||
chr13:102852815 | T | A | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.264+522T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852815 | |||||||
chr13:102852891 | G | A | 1 | a0002c0002t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.264+598G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852891 | |||||||
chr13:102852963 | C | A | 1 | a0023c0036t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.264+670C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102852963 | |||||||
chr13:102853061 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.265-696A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102853061 | |||||||
chr13:102853321 | A | G | 10 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(7): Show |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.265-436A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | chr13 | 102853321 | |||||||
chr13:102853572 | ACT | A | 8 | a0003c0006t0003g0016 a0003c0006t0003g0034 a0003c0006t0003g0103 others(5): Show |
12 | HG02015.hp2 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.265-182_265-181del others(2): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 102853572 | ||||||
chr13:102853942 | G | A | 2 | a0001c0001t0008g0064 a0003c0006t0006g0098 |
2 | HG01069.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.380+70G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | chr13 | 102853942 | |||||||
chr13:102854012 | AT | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.380+144delT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 102854012 | ||||||
chr13:102854033 | G | A | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.380+161G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | chr13 | 102854033 | |||||||
chr13:102854089 | G | A | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-199G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | chr13 | 102854089 | |||||||
chr13:102854099 | G | A | 1 | a0002c0002t0002g0171 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.381-189G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | chr13 | 102854099 | |||||||
chr13:102854142 | G | A | 1 | a0002c0004t0002g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381-146G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | chr13 | 102854142 | |||||||
chr13:102854159 | A | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.381-129A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 3/14 | chr13 | 102854159 | |||||||
chr13:102854485 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.467+111T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102854485 | |||||||
chr13:102854699 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.467+325G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102854699 | |||||||
chr13:102854761 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(160): Show |
221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.467+387T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102854761 | |||||||
chr13:102854778 | G | A | 14 | a0003c0006t0003g0016 a0003c0006t0003g0034 a0003c0006t0003g0103 others(11): Show |
18 | HG01069.hp2 HG02015.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.467+404G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102854778 | |||||||
chr13:102854843 | C | T | 1 | a0004c0007t0004g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.467+469C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102854843 | |||||||
chr13:102854879 | T | A | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.467+505T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102854879 | |||||||
chr13:102855240 | C | T | 1 | a0002c0005t0002g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.468-812C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855240 | |||||||
chr13:102855282 | C | T | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.468-770C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855282 | |||||||
chr13:102855310 | C | T | 1 | a0002c0005t0002g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468-742C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855310 | |||||||
chr13:102855363 | C | T | 1 | a0002c0002t0002g0167 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.468-689C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855363 | |||||||
chr13:102855372 | C | A | 8 | a0003c0006t0003g0016 a0003c0006t0003g0034 a0003c0006t0003g0103 others(5): Show |
12 | HG02015.hp2 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.468-680C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855372 | |||||||
chr13:102855403 | C | T | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.468-649C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855403 | |||||||
chr13:102855668 | C | T | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.468-384C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855668 | |||||||
chr13:102855692 | G | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0002c0002t0002g0132 |
3 | NA18947.hp2 NA18998.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.468-360G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855692 | |||||||
chr13:102855717 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.468-335C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855717 | |||||||
chr13:102855718 | G | A | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.468-334G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855718 | |||||||
chr13:102855745 | G | A | 30 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(27): Show |
51 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.468-307G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855745 | |||||||
chr13:102855962 | C | T | 1 | a0002c0002t0002g0044 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.468-90C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 4/14 | chr13 | 102855962 | |||||||
chr13:102856156 | A | T | 1 | a0002c0004t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528+44A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856156 | |||||||
chr13:102856157 | A | C | 1 | a0002c0004t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528+45A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856157 | |||||||
chr13:102856297 | G | GTA | 161 | a0001c0001t0001g0026 a0001c0001t0001g0130 a0001c0001t0001g0131 others(158): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.528+199_528+200dup others(2): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr13 | 102856297 | ||||||
chr13:102856297 | G | GTATA | 10 | a0001c0003t0001g0013 a0002c0002t0002g0133 a0002c0004t0002g0112 others(7): Show |
24 | HG01975.hp1 HG02040.hp2 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.528+197_528+200dup others(4): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr13 | 102856297 | ||||||
chr13:102856323 | A | G | 1 | a0001c0003t0003g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.528+211A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856323 | |||||||
chr13:102856580 | C | T | 66 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(63): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.528+468C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856580 | |||||||
chr13:102856581 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.528+469G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856581 | |||||||
chr13:102856727 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.528+615T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856727 | |||||||
chr13:102856782 | G | A | 5 | a0003c0006t0006g0098 a0003c0006t0006g0100 a0003c0006t0006g0101 others(2): Show |
5 | HG01069.hp2 HG03654.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+670G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856782 | |||||||
chr13:102856810 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.528+698C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856810 | |||||||
chr13:102856817 | C | T | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.528+705C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856817 | |||||||
chr13:102856822 | C | A | 1 | a0002c0002t0002g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.528+710C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856822 | |||||||
chr13:102856829 | A | T | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.528+717A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102856829 | |||||||
chr13:102857056 | T | C | 1 | a0002c0004t0002g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.528+944T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857056 | |||||||
chr13:102857115 | C | T | 1 | a0005c0009t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.528+1003C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857115 | |||||||
chr13:102857238 | A | T | 1 | a0002c0002t0002g0043 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.529-1037A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857238 | |||||||
chr13:102857249 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.529-1026G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857249 | |||||||
chr13:102857293 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.529-982C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857293 | |||||||
chr13:102857318 | A | T | 12 | a0001c0003t0001g0006 a0001c0003t0001g0032 a0001c0003t0001g0080 others(9): Show |
17 | HG00597.hp1 HG01975.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.529-957A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857318 | |||||||
chr13:102857388 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.529-887T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857388 | |||||||
chr13:102857629 | T | TCTTA | 104 | a0001c0001t0008g0064 a0001c0003t0001g0001 a0001c0003t0001g0006 others(101): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.529-643_529-642ins others(4): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr13 | 102857629 | ||||||
chr13:102857649 | T | C | 1 | a0002c0002t0002g0170 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.529-626T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857649 | |||||||
chr13:102857866 | T | C | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.529-409T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857866 | |||||||
chr13:102857988 | A | G | 1 | a0002c0002t0002g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.529-287A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857988 | |||||||
chr13:102857996 | C | T | 3 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 |
4 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-279C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 5/14 | chr13 | 102857996 | |||||||
chr13:102858533 | A | C | 3 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 |
4 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+115A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858533 | |||||||
chr13:102858546 | C | T | 102 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(99): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.672+128C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858546 | |||||||
chr13:102858647 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.672+229T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858647 | |||||||
chr13:102858861 | A | C | 22 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(19): Show |
39 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+443A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858861 | |||||||
chr13:102858945 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.672+527A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858945 | |||||||
chr13:102858951 | T | C | 98 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(95): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.672+533T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858951 | |||||||
chr13:102858969 | C | G | 1 | a0001c0003t0002g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.672+551C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858969 | |||||||
chr13:102858986 | G | A | 2 | a0008c0013t0002g0023 a0008c0019t0002g0023 |
3 | HG01884.hp2 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.672+568G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102858986 | |||||||
chr13:102859078 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(160): Show |
221 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.672+660G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859078 | |||||||
chr13:102859122 | A | G | 19 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(16): Show |
37 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.672+704A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859122 | |||||||
chr13:102859138 | C | G | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672+720C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859138 | |||||||
chr13:102859232 | C | A | 20 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(17): Show |
35 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.672+814C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859232 | |||||||
chr13:102859281 | T | TA | 1 | a0009c0012t0002g0028 | 3 | HG02135.hp2 NA19062.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.672+864dupA | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 102859281 | ||||||
chr13:102859372 | T | C | 1 | a0002c0002t0002g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.672+954T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859372 | |||||||
chr13:102859409 | C | G | 1 | a0010c0015t0001g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.672+991C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859409 | |||||||
chr13:102859743 | G | A | 3 | a0004c0007t0002g0045 a0004c0007t0002g0191 a0004c0007t0002g0192 |
4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+1325G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859743 | |||||||
chr13:102859797 | T | C | 2 | a0002c0002t0002g0036 a0002c0002t0002g0135 |
3 | HG00408.hp1 NA18966.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.672+1379T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859797 | |||||||
chr13:102859822 | T | C | 3 | a0001c0001t0005g0046 a0001c0001t0005g0197 a0001c0001t0005g0249 |
4 | HG02145.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+1404T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859822 | |||||||
chr13:102859928 | T | C | 52 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(49): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.672+1510T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859928 | |||||||
chr13:102859931 | A | G | 1 | a0002c0004t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672+1513A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859931 | |||||||
chr13:102859961 | A | T | 1 | a0001c0003t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.672+1543A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859961 | |||||||
chr13:102859982 | C | G | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.673-1525C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102859982 | |||||||
chr13:102860079 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.673-1428G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860079 | |||||||
chr13:102860154 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(177): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.673-1353C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860154 | |||||||
chr13:102860356 | G | C | 1 | a0018c0020t0002g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.673-1151G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860356 | |||||||
chr13:102860509 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.673-998A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860509 | |||||||
chr13:102860577 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.673-930G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860577 | |||||||
chr13:102860728 | G | T | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.673-779G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860728 | |||||||
chr13:102860877 | A | G | 1 | a0002c0004t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673-630A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102860877 | |||||||
chr13:102860986 | AT | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(246): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-502delT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 102860986 | ||||||
chr13:102860986 | ATT | A | 13 | a0001c0003t0001g0080 a0002c0004t0002g0008 a0002c0004t0002g0035 others(10): Show |
16 | HG01192.hp1 HG01975.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.673-503_673-502del others(2): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 102860986 | ||||||
chr13:102861009 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.673-498G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102861009 | |||||||
chr13:102861018 | C | T | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.673-489C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102861018 | |||||||
chr13:102861074 | T | G | 1 | a0001c0003t0001g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.673-433T>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102861074 | |||||||
chr13:102861191 | G | A | 1 | a0003c0006t0007g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.673-316G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102861191 | |||||||
chr13:102861228 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.673-279G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102861228 | |||||||
chr13:102861473 | A | G | 1 | a0018c0020t0002g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.673-34A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 6/14 | chr13 | 102861473 | |||||||
chr13:102861741 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.880+27T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/14 | chr13 | 102861741 | |||||||
chr13:102861910 | C | T | 1 | a0001c0003t0001g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.881-120C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/14 | chr13 | 102861910 | |||||||
chr13:102862000 | A | G | 1 | a0001c0003t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.881-30A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 7/14 | chr13 | 102862000 | |||||||
chr13:102863137 | G | A | 1 | a0002c0002t0002g0137 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1954+34G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863137 | |||||||
chr13:102863139 | T | C | 3 | a0002c0002t0002g0183 a0002c0002t0002g0184 a0002c0002t0002g0185 |
3 | HG01891.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1954+36T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863139 | |||||||
chr13:102863211 | C | G | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1954+108C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863211 | |||||||
chr13:102863211 | C | T | 16 | a0003c0006t0003g0016 a0003c0006t0003g0034 a0003c0006t0003g0103 others(13): Show |
21 | HG01069.hp2 HG01884.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1954+108C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863211 | |||||||
chr13:102863532 | C | A | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1954+429C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863532 | |||||||
chr13:102863642 | C | T | 39 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0013 others(36): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1954+539C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863642 | |||||||
chr13:102863700 | C | T | 2 | a0002c0004t0002g0089 a0002c0004t0002g0093 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1954+597C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863700 | |||||||
chr13:102863891 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0025t0001g0198 |
3 | HG00733.hp1 HG01361.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1954+788G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102863891 | |||||||
chr13:102864026 | A | G | 1 | a0003c0006t0003g0106 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1954+923A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864026 | |||||||
chr13:102864126 | C | CCA | 8 | a0001c0001t0001g0189 a0001c0003t0001g0075 a0001c0003t0001g0078 others(5): Show |
8 | HG01081.hp1 HG01993.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1954+1062_1954+106 others(6): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACA | 57 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0145 others(54): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1954+1060_1954+106 others(8): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACA | 18 | a0001c0001t0001g0026 a0001c0001t0001g0110 a0001c0001t0001g0136 others(15): Show |
20 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1954+1058_1954+106 others(10): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(1): Show |
34 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0199 others(31): Show |
47 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1954+1056_1954+106 others(12): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(3): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(21): Show |
42 | HG01074.hp2 HG01106.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.1954+1054_1954+106 others(14): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(5): Show |
22 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0190 others(19): Show |
36 | HG00408.hp2 HG01069.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1954+1052_1954+106 others(16): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(7): Show |
12 | a0001c0001t0001g0011 a0001c0001t0001g0111 a0001c0001t0001g0211 others(9): Show |
17 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1954+1050_1954+106 others(18): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(9): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
11 | HG00438.hp2 HG00558.hp1 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.1954+1048_1954+106 others(20): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(11): Show |
1 | a0001c0001t0001g0052 | 2 | NA19066.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1954+1046_1954+106 others(22): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(13): Show |
2 | a0001c0001t0001g0053 a0001c0037t0001g0217 |
3 | NA18942.hp2 NA18956.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1954+1044_1954+106 others(24): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(15): Show |
1 | a0001c0001t0001g0218 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1954+1042_1954+106 others(26): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | C | CCACACAC others(17): Show |
1 | a0001c0001t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1954+1040_1954+106 others(28): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | CCA | C | 25 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0013 others(22): Show |
51 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1954+1062_1954+106 others(6): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | CCACA | C | 4 | a0001c0003t0001g0032 a0001c0003t0001g0068 a0002c0002t0002g0229 others(1): Show |
7 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1954+1060_1954+106 others(8): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | CCACACA | C | 23 | a0002c0002t0005g0236 a0003c0006t0003g0016 a0003c0006t0003g0034 others(20): Show |
31 | HG01069.hp2 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1954+1058_1954+106 others(10): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | CCACACAC others(3): Show |
C | 1 | a0002c0005t0002g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1954+1054_1954+106 others(14): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864126 | CCACACAC others(5): Show |
C | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1954+1052_1954+106 others(16): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 102864126 | ||||||
chr13:102864427 | C | G | 1 | a0003c0006t0003g0106 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1955-1240C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864427 | |||||||
chr13:102864457 | T | A | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1955-1210T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864457 | |||||||
chr13:102864495 | A | G | 1 | a0001c0003t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1955-1172A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864495 | |||||||
chr13:102864701 | G | A | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1955-966G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864701 | |||||||
chr13:102864780 | A | G | 52 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(49): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1955-887A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864780 | |||||||
chr13:102864797 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1955-870G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864797 | |||||||
chr13:102864959 | C | T | 1 | a0002c0002t0002g0132 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1955-708C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102864959 | |||||||
chr13:102865032 | T | C | 2 | a0002c0002t0002g0141 a0002c0002t0002g0142 |
2 | NA18952.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1955-635T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102865032 | |||||||
chr13:102865112 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(251): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1955-555T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102865112 | |||||||
chr13:102865257 | C | T | 10 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(7): Show |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1955-410C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102865257 | |||||||
chr13:102865292 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.1955-375A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102865292 | |||||||
chr13:102865329 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1955-338G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102865329 | |||||||
chr13:102865520 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1955-147C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 8/14 | chr13 | 102865520 | |||||||
chr13:102865987 | G | A | 2 | a0001c0003t0002g0091 a0001c0003t0003g0092 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2199+76G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 9/14 | chr13 | 102865987 | |||||||
chr13:102866066 | G | C | 2 | a0008c0013t0002g0023 a0008c0019t0002g0023 |
3 | HG01884.hp2 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2199+155G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 9/14 | chr13 | 102866066 | |||||||
chr13:102866116 | CAG | C | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2200-143_2200-142d others(4): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr13 | 102866116 | ||||||
chr13:102866158 | A | G | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0196 others(5): Show |
10 | NA18949.hp2 NA18950.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.2200-104A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 9/14 | chr13 | 102866158 | |||||||
chr13:102866419 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2319+38T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 10/14 | chr13 | 102866419 | |||||||
chr13:102866425 | C | T | 10 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(7): Show |
13 | HG01192.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2319+44C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 10/14 | chr13 | 102866425 | |||||||
chr13:102866465 | G | C | 2 | a0002c0005t0002g0024 a0002c0005t0002g0120 |
4 | HG01975.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+84G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 10/14 | chr13 | 102866465 | |||||||
chr13:102866494 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(71): Show |
111 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.2319+113C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 10/14 | chr13 | 102866494 | |||||||
chr13:102866901 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0209 a0001c0001t0001g0230 |
3 | HG00642.hp2 HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2533+56C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102866901 | |||||||
chr13:102867080 | G | C | 1 | a0002c0002t0002g0179 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2533+235G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867080 | |||||||
chr13:102867111 | A | G | 1 | a0009c0012t0002g0028 | 3 | HG02135.hp2 NA19062.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2533+266A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867111 | |||||||
chr13:102867120 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(72): Show |
112 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.2533+275G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867120 | |||||||
chr13:102867421 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2533+576G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867421 | |||||||
chr13:102867842 | A | G | 9 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(6): Show |
13 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2534-271A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867842 | |||||||
chr13:102867860 | G | C | 1 | a0002c0002t0002g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2534-253G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867860 | |||||||
chr13:102867901 | T | C | 12 | a0001c0003t0001g0006 a0001c0003t0001g0032 a0001c0003t0001g0080 others(9): Show |
17 | HG00597.hp1 HG01975.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.2534-212T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102867901 | |||||||
chr13:102868026 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2534-87C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102868026 | |||||||
chr13:102868030 | C | T | 2 | a0002c0004t0002g0089 a0002c0004t0002g0093 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2534-83C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 11/14 | chr13 | 102868030 | |||||||
chr13:102868316 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2678+59G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868316 | |||||||
chr13:102868348 | G | A | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2678+91G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868348 | |||||||
chr13:102868414 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2678+157G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868414 | |||||||
chr13:102868620 | C | A | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2678+363C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868620 | |||||||
chr13:102868621 | C | T | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2678+364C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868621 | |||||||
chr13:102868764 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(158): Show |
219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2678+507C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868764 | |||||||
chr13:102868795 | A | T | 3 | a0001c0001t0005g0046 a0001c0001t0005g0197 a0001c0001t0005g0249 |
4 | HG02145.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2678+538A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102868795 | |||||||
chr13:102869032 | G | A | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2678+775G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869032 | |||||||
chr13:102869080 | T | A | 1 | a0002c0004t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2678+823T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869080 | |||||||
chr13:102869185 | T | A | 1 | a0003c0006t0003g0107 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2678+928T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869185 | |||||||
chr13:102869222 | A | G | 1 | a0003c0006t0006g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2678+965A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869222 | |||||||
chr13:102869236 | A | G | 1 | a0002c0004t0002g0035 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2678+979A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869236 | |||||||
chr13:102869278 | G | T | 36 | a0001c0001t0001g0203 a0001c0003t0001g0001 a0001c0003t0001g0006 others(33): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2678+1021G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869278 | |||||||
chr13:102869293 | G | A | 11 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(8): Show |
14 | HG01192.hp1 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2678+1036G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869293 | |||||||
chr13:102869325 | G | A | 52 | a0001c0001t0001g0203 a0001c0003t0001g0001 a0001c0003t0001g0006 others(49): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2678+1068G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869325 | |||||||
chr13:102869385 | A | G | 4 | a0002c0002t0002g0137 a0002c0002t0002g0156 a0002c0002t0002g0157 others(1): Show |
4 | NA19058.hp1 NA19075.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.2678+1128A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869385 | |||||||
chr13:102869413 | G | A | 1 | a0001c0001t0001g0047 | 2 | NA19012.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2678+1156G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869413 | |||||||
chr13:102869437 | T | C | 1 | a0001c0008t0001g0208 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2678+1180T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869437 | |||||||
chr13:102869450 | A | ACTTCT | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2678+1197_2678+119 others(9): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 102869450 | ||||||
chr13:102869488 | G | A | 1 | a0001c0003t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2678+1231G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869488 | |||||||
chr13:102869495 | C | A | 1 | a0002c0004t0002g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2678+1238C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869495 | |||||||
chr13:102869958 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2678+1701G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102869958 | |||||||
chr13:102870206 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2678+1949A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870206 | |||||||
chr13:102870209 | C | T | 1 | a0002c0004t0002g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2678+1952C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870209 | |||||||
chr13:102870311 | G | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2679-1887G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870311 | |||||||
chr13:102870420 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2679-1778G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870420 | |||||||
chr13:102870617 | A | C | 7 | a0001c0003t0001g0007 a0001c0003t0001g0033 a0001c0003t0001g0088 others(4): Show |
13 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.2679-1581A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870617 | |||||||
chr13:102870685 | A | T | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2679-1513A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870685 | |||||||
chr13:102870717 | A | G | 10 | a0002c0002t0002g0129 a0002c0002t0002g0134 a0002c0002t0002g0137 others(7): Show |
10 | HG01952.hp1 NA18940.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.2679-1481A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870717 | |||||||
chr13:102870773 | A | C | 1 | a0009c0012t0002g0028 | 3 | HG02135.hp2 NA19062.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2679-1425A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870773 | |||||||
chr13:102870796 | C | G | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2679-1402C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870796 | |||||||
chr13:102870888 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2679-1310A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870888 | |||||||
chr13:102870962 | C | T | 39 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0013 others(36): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.2679-1236C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102870962 | |||||||
chr13:102871055 | G | GT | 9 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(6): Show |
13 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2679-1142dupT | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 102871055 | ||||||
chr13:102871083 | C | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(255): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.2679-1115C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871083 | |||||||
chr13:102871160 | C | T | 1 | a0003c0006t0006g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2679-1038C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871160 | |||||||
chr13:102871192 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2679-1006A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871192 | |||||||
chr13:102871207 | C | G | 10 | a0004c0007t0002g0010 a0004c0007t0002g0045 a0004c0007t0002g0191 others(7): Show |
16 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.2679-991C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871207 | |||||||
chr13:102871293 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2679-905G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871293 | |||||||
chr13:102871297 | T | TCTTGAGC others(4): Show |
1 | a0002c0002t0002g0143 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2679-901_2679-900i others(13): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871297 | |||||||
chr13:102871472 | G | A | 5 | a0002c0005t0002g0003 a0002c0005t0002g0115 a0002c0005t0002g0121 others(2): Show |
14 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2679-726G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871472 | |||||||
chr13:102871494 | T | C | 2 | a0001c0003t0002g0091 a0001c0003t0003g0092 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2679-704T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871494 | |||||||
chr13:102871619 | TTA | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2679-568_2679-567d others(4): Show |
ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 102871619 | ||||||
chr13:102871696 | A | G | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2679-502A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871696 | |||||||
chr13:102871733 | C | T | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2679-465C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871733 | |||||||
chr13:102871886 | C | T | 1 | a0001c0003t0001g0084 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2679-312C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871886 | |||||||
chr13:102871999 | G | A | 14 | a0003c0006t0003g0016 a0003c0006t0003g0034 a0003c0006t0003g0103 others(11): Show |
18 | HG01069.hp2 HG02015.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.2679-199G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102871999 | |||||||
chr13:102872023 | G | A | 3 | a0001c0001t0008g0064 a0007c0010t0002g0019 a0007c0010t0002g0062 |
5 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679-175G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102872023 | |||||||
chr13:102872082 | G | A | 7 | a0002c0005t0002g0003 a0002c0005t0002g0024 a0002c0005t0002g0115 others(4): Show |
18 | HG01975.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2679-116G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 12/14 | chr13 | 102872082 | |||||||
chr13:102872412 | C | T | 51 | a0001c0003t0001g0001 a0001c0003t0001g0006 a0001c0003t0001g0007 others(48): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2879+14C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872412 | |||||||
chr13:102872604 | A | C | 32 | a0002c0004t0002g0008 a0002c0004t0002g0035 a0002c0004t0002g0113 others(29): Show |
50 | HG01069.hp2 HG01192.hp1 HG01975.hp1 others(47): Show |
intron_variant | MODIFIER | c.2879+206A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872604 | |||||||
chr13:102872673 | A | G | 1 | a0001c0001t0001g0047 | 2 | NA19012.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2879+275A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872673 | |||||||
chr13:102872773 | G | A | 1 | a0001c0003t0002g0022 | 3 | HG00639.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2879+375G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872773 | |||||||
chr13:102872774 | C | A | 4 | a0001c0003t0003g0055 a0001c0003t0003g0248 a0016c0023t0003g0247 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2879+376C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872774 | |||||||
chr13:102872855 | G | C | 1 | a0002c0002t0002g0141 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2880-404G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872855 | |||||||
chr13:102872932 | G | C | 4 | a0002c0002t0005g0236 a0003c0006t0003g0034 a0003c0006t0003g0103 others(1): Show |
5 | NA18947.hp1 NA18974.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.2880-327G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102872932 | |||||||
chr13:102873073 | T | C | 2 | a0002c0004t0002g0089 a0002c0004t0002g0093 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2880-186T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 13/14 | chr13 | 102873073 | |||||||
chr13:102873468 | G | C | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2964+125G>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102873468 | |||||||
chr13:102873533 | C | A | 1 | a0002c0029t0002g0161 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2964+190C>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102873533 | |||||||
chr13:102873643 | G | A | 2 | a0002c0004t0002g0089 a0002c0004t0002g0093 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2964+300G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102873643 | |||||||
chr13:102873663 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2964+320C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102873663 | |||||||
chr13:102873789 | T | C | 89 | a0001c0001t0001g0026 a0001c0001t0001g0130 a0001c0001t0001g0131 others(86): Show |
110 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2964+446T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102873789 | |||||||
chr13:102874059 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2964+716T>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874059 | |||||||
chr13:102874312 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(263): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2964+969G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874312 | |||||||
chr13:102874484 | A | G | 1 | a0001c0008t0002g0049 | 2 | NA18995.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2965-823A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874484 | |||||||
chr13:102874531 | T | A | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2965-776T>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874531 | |||||||
chr13:102874553 | A | G | 2 | a0002c0002t0002g0152 a0002c0002t0002g0155 |
2 | NA18940.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2965-754A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874553 | |||||||
chr13:102874555 | T | C | 1 | a0002c0002t0002g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2965-752T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874555 | |||||||
chr13:102874561 | T | G | 5 | a0001c0001t0001g0202 a0001c0001t0001g0209 a0001c0001t0001g0230 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2965-746T>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874561 | |||||||
chr13:102874582 | T | C | 1 | a0002c0002t0002g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2965-725T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874582 | |||||||
chr13:102874584 | A | C | 1 | a0002c0002t0002g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2965-723A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874584 | |||||||
chr13:102874587 | A | T | 1 | a0002c0002t0002g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2965-720A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874587 | |||||||
chr13:102874606 | C | T | 1 | a0001c0001t0008g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2965-701C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874606 | |||||||
chr13:102874670 | C | T | 2 | a0002c0004t0002g0089 a0002c0004t0002g0093 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2965-637C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874670 | |||||||
chr13:102874676 | C | T | 1 | a0002c0002t0002g0132 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2965-631C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874676 | |||||||
chr13:102874677 | A | G | 3 | a0001c0001t0001g0131 a0002c0002t0002g0132 a0003c0022t0003g0097 |
3 | NA18947.hp2 NA18998.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2965-630A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874677 | |||||||
chr13:102874682 | T | C | 5 | a0001c0003t0001g0081 a0002c0002t0002g0132 a0002c0002t0002g0138 others(2): Show |
5 | HG02735.hp2 HG03516.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.2965-625T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874682 | |||||||
chr13:102874713 | C | G | 1 | a0002c0004t0002g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2965-594C>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874713 | |||||||
chr13:102874713 | C | T | 1 | a0019c0021t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2965-594C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874713 | |||||||
chr13:102874715 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2965-592G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874715 | |||||||
chr13:102874717 | G | A | 2 | a0002c0002t0002g0144 a0002c0002t0002g0188 |
2 | HG02071.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2965-590G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874717 | |||||||
chr13:102874724 | C | T | 5 | a0002c0002t0002g0041 a0002c0002t0002g0140 a0002c0002t0002g0141 others(2): Show |
5 | HG02015.hp1 HG04228.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2965-583C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874724 | |||||||
chr13:102874725 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02132.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2965-582G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874725 | |||||||
chr13:102874725 | G | T | 1 | a0002c0002t0002g0044 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2965-582G>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874725 | |||||||
chr13:102874729 | A | C | 1 | a0001c0003t0001g0087 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2965-578A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874729 | |||||||
chr13:102874729 | A | T | 62 | a0001c0001t0001g0136 a0001c0001t0001g0190 a0001c0001t0001g0200 others(59): Show |
73 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2965-578A>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874729 | |||||||
chr13:102874734 | A | G | 1 | a0001c0008t0002g0049 | 2 | NA18995.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2965-573A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874734 | |||||||
chr13:102874736 | A | G | 32 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0130 others(29): Show |
38 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2965-571A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874736 | |||||||
chr13:102874740 | G | A | 3 | a0001c0008t0001g0208 a0001c0008t0001g0228 a0003c0006t0003g0103 |
3 | NA18948.hp1 NA18998.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2965-567G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874740 | |||||||
chr13:102874745 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2965-562G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874745 | |||||||
chr13:102874756 | G | A | 1 | a0014c0034t0002g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2965-551G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874756 | |||||||
chr13:102874763 | A | G | 84 | a0001c0001t0001g0047 a0001c0001t0001g0130 a0001c0001t0001g0131 others(81): Show |
102 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2965-544A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874763 | |||||||
chr13:102874767 | A | G | 82 | a0001c0001t0001g0047 a0001c0001t0001g0130 a0001c0001t0001g0131 others(79): Show |
100 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.2965-540A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874767 | |||||||
chr13:102874771 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(257): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.2965-536C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874771 | |||||||
chr13:102874791 | G | A | 60 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0190 others(57): Show |
76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2965-516G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874791 | |||||||
chr13:102874796 | A | C | 1 | a0002c0004t0002g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2965-511A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874796 | |||||||
chr13:102874799 | C | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(211): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.2965-508C>T | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874799 | |||||||
chr13:102874810 | A | G | 10 | a0001c0001t0001g0131 a0001c0001t0002g0225 a0001c0003t0001g0073 others(7): Show |
10 | HG01243.hp2 HG02809.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2965-497A>G | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874810 | |||||||
chr13:102874811 | T | C | 10 | a0001c0001t0001g0131 a0001c0001t0002g0225 a0001c0003t0001g0073 others(7): Show |
10 | HG01243.hp2 HG02809.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2965-496T>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874811 | |||||||
chr13:102874874 | AC | A | 2 | a0007c0010t0002g0019 a0007c0010t0002g0062 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2965-432delC | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874874 | |||||||
chr13:102874880 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0048 others(17): Show |
32 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2965-427G>A | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102874880 | |||||||
chr13:102875178 | A | C | 9 | a0001c0003t0001g0015 a0001c0003t0001g0021 a0001c0003t0001g0065 others(6): Show |
13 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2965-129A>C | ERCC5 | ENSG00000134899.24 | transcript | ENST00000652225.2 | protein_coding | 14/14 | chr13 | 102875178 |