Bibliome.ai browser hg19
Search
About
Stats
FAQ
KCNH2 c.2054G>A ;(p.R685H)
Variant ID: 7-150648100-C-T
NM_000238.3(
KCNH2
):c.2054G>A;(p.R685H)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Assessment of absolute risk of life-threatening cardiac events in long QT syndrome patients.
Frontiers In Cardiovascular Medicine
Wang, Meng M; Peterson, Derick R DR; Pagan, Eleonora E; Bagnardi, Vincenzo V; Mazzanti, Andrea A; McNitt, Scott S; Rich, David Q DQ; Seplaki, Christopher L CL; Kutyifa, Valentina V; Polonsky, Bronislava B; Barsheshet, Alon A; Kukavica, Deni D; Rosero, Spencer S; Goldenberg, Ilan I; Priori, Silvia S; Zareba, Wojciech W
Publication Date: 2022
Variant appearance in text: LQT2: R685H
PubMed Link:
36277779
Variant Present in the following documents:
Data_Sheet_1.pdf
View BVdb publication page
Structures Illuminate Cardiac Ion Channel Functions in Health and in Long QT Syndrome.
Frontiers In Pharmacology
Brewer, Kathryn R KR; Kuenze, Georg G; Vanoye, Carlos G CG; George, Alfred L AL; Meiler, Jens J; Sanders, Charles R CR
Publication Date: 2020
Variant appearance in text: LQT2: R685H
PubMed Link:
32431610
Variant Present in the following documents:
Main text
View BVdb publication page