APP c.2131G>T ;(p.V711F)

Variant ID: 21-27264114-C-A

NM_000484.3(APP):c.2131G>T;(p.V711F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of genetic polymorphisms in unexplained recurrent spontaneous abortion based on whole exome sequencing.

Annals Of Translational Medicine
Mou, Jiang-Tao JT; Huang, Shi-Xing SX; Yu, Li-Li LL; Xu, Jing J; Deng, Qiao-Ling QL; Xie, Yi-Shan YS; Deng, Kun K
Publication Date: 2022-05

Variant appearance in text: APP: 2131G>T; V711F
PubMed Link: 35722368
Variant Present in the following documents:
  • Main text
  • atm-10-10-603.pdf
View BVdb publication page



Effect of anti-inflammatory agents on transforming growth factor beta over-expressing mouse brains: a model revised.

Journal Of Neuroinflammation
Lacombe, Pierre P; Mathews, Paul M PM; Schmidt, Stephen D SD; Breidert, Tilo T; Heneka, Michael T MT; Landreth, Gary E GE; Feinstein, Douglas L DL; Galea, Elena E
Publication Date: 2004-07-02

Variant appearance in text: APP: V711F
PubMed Link: 15285804
Variant Present in the following documents:
  • Main text
  • 1742-2094-1-11.pdf
View BVdb publication page