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.




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