KCNH2 c.2452T>C ;(p.S818P)

Variant ID: 7-150646084-A-G

NM_000238.3(KCNH2):c.2452T>C;(p.S818P)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole-exome sequencing.

Journal Of Arrhythmia
Fazelifar, Amir Farjam AF; Pourirahim, Maryam M; Masoumi, Tannaz T; Biglari, Alireza A; Maleki, Majid M; Kalayinia, Samira S
Publication Date: 2023-06

Variant appearance in text: KCNH2: S818P; rs199473537
PubMed Link: 37324772
Variant Present in the following documents:
  • Main text
  • JOA3-39-430.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: S818P
PubMed Link: 32431610
Variant Present in the following documents:
  • Main text
View BVdb publication page



The enigmatic cytoplasmic regions of KCNH channels.

Journal Of Molecular Biology
Morais-Cabral, João H JH; Robertson, Gail A GA
Publication Date: 2015-01-16

Variant appearance in text: LQT2: S818P
PubMed Link: 25158096
Variant Present in the following documents:
  • Main text
View BVdb publication page