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ERCC8 c.1122+1767A>T
Variant ID: 5-60181500-T-A
NM_000082.3(
ERCC8
):c.1122+1767A>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A.
Scientific Reports
Wang, Xiaozhu X; Huang, Yu Y; Yan, Ming M; Li, Jiuwei J; Ding, Changhong C; Jin, Hong H; Fang, Fang F; Yang, Yanling Y; Wu, Baiyan B; Chen, Dafang D
Publication Date: 2017-10-20
Variant appearance in text: rs12522154
PubMed Link:
29057985
Variant Present in the following documents:
Main text
41598_2017_Article_14034.pdf
View BVdb publication page