CD4 c.878G>A ;(p.G293D)

Variant ID: 12-6925492-G-A

NM_000616.4(CD4):c.878G>A;(p.G293D)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Case Report: The novel hemizygous mutation in the SSR4 gene caused congenital disorder of glycosylation type iy: A case study and literature review.

Frontiers In Genetics
Wang, Jun J; Gou, Xingqing X; Wang, Xiyi X; Zhang, Jing J; Zhao, Nan N; Wang, Xiaohong X
Publication Date: 2022

Variant appearance in text: CD4: 878G>A
PubMed Link: 36386804
Variant Present in the following documents:
  • Table1.xls, sheet 2
View BVdb publication page



Histamine H(3) receptor integrates peripheral inflammatory signals in the neurogenic control of immune responses and autoimmune disease susceptibility.

Plos One
Krementsov, Dimitry N DN; Wall, Emma H EH; Martin, Rebecca A RA; Subramanian, Meenakumari M; Noubade, Rajkumar R; Del Rio, Roxana R; Mawe, Gary M GM; Bond, Jeffrey P JP; Poynter, Matthew E ME; Blankenhorn, Elizabeth P EP; Teuscher, Cory C
Publication Date: 2013

Variant appearance in text: CD4: G293D
PubMed Link: 23894272
Variant Present in the following documents:
  • Main text
View BVdb publication page