NSF c.1126C>G ;(p.P376A)

Variant ID: 17-44771227-C-G

NM_006178.3(NSF):c.1126C>G;(p.P376A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Characterizing microRNA editing and mutation sites in Autism Spectrum Disorder.

Frontiers In Molecular Neuroscience
Wu, Xingwang X; Yang, Huaide H; Lin, Han H; Suo, Angbaji A; Wu, Shuai S; Xie, Wenping W; Zhou, Nan N; Guo, Shiyong S; Ding, Hao H; Zhou, Guangchen G; Qiu, Zhichao Z; Shi, Hong H; Yang, Jun J; Zheng, Yun Y
Publication Date: 2022

Variant appearance in text: NSF: p376a
PubMed Link: 36743290
Variant Present in the following documents:
  • Main text
  • fnmol-15-1105278.pdf
View BVdb publication page



Endosomal system genetics and autism spectrum disorders: A literature review.

Neuroscience And Biobehavioral Reviews
Patak, Jameson J; Zhang-James, Yanli Y; Faraone, Stephen V SV
Publication Date: 2016-06

Variant appearance in text: NSF: 1126C>G
PubMed Link: 27048963
Variant Present in the following documents:
  • Main text
View BVdb publication page