KCNH2 c.3146T>C ;(p.L1049P)

Variant ID: 7-150644422-A-G

NM_000238.3(KCNH2):c.3146T>C;(p.L1049P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating.

International Journal Of Molecular Sciences
Farrugia, Audrey A; Rollet, Kevin K; Sinniger, Jérome J; Brun, Susana S; Spenle, Caroline C; Ludes, Bertrand B; Taleb, Omar O; Mensah-Nyagan, Ayikoe Guy AG
Publication Date: 2021-08-26

Variant appearance in text: Kv11.1: L1049P
PubMed Link: 34502138
Variant Present in the following documents:
  • Main text
  • ijms-22-09235.pdf
View BVdb publication page



Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome.

Nature Communications
Anderson, Corey L CL; Kuzmicki, Catherine E CE; Childs, Ryan R RR; Hintz, Caleb J CJ; Delisle, Brian P BP; January, Craig T CT
Publication Date: 2014-11-24

Variant appearance in text: LQT2: L1049P
PubMed Link: 25417810
Variant Present in the following documents:
  • Main text
  • nihms634670.pdf
View BVdb publication page