KCNH2 c.2246G>C ;(p.G749A)

Variant ID: 7-150647408-C-G

NM_000238.3(KCNH2):c.2246G>C;(p.G749A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Loss-of-function variants in Kv 11.1 cardiac channels as a biomarker for SUDEP.

Annals Of Clinical And Translational Neurology
Soh, Ming S MS; Bagnall, Richard D RD; Bennett, Mark F MF; Bleakley, Lauren E LE; Mohamed Syazwan, Erlina S ES; Phillips, A Marie AM; Chiam, Mathew D F MDF; McKenzie, Chaseley E CE; Hildebrand, Michael M; Crompton, Douglas D; Bahlo, Melanie M; Semsarian, Christopher C; Scheffer, Ingrid E IE; Berkovic, Samuel F SF; Reid, Christopher A CA
Publication Date: 2021-07

Variant appearance in text: KCNH2: G749A
PubMed Link: 34002542
Variant Present in the following documents:
  • Main text
  • ACN3-8-1422.pdf
View BVdb publication page



Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?

Frontiers In Neurology
Bleakley, Lauren E LE; Soh, Ming S MS; Bagnall, Richard D RD; Sadleir, Lynette G LG; Gooley, Samuel S; Semsarian, Christopher C; Scheffer, Ingrid E IE; Berkovic, Samuel F SF; Reid, Christopher A CA
Publication Date: 2020

Variant appearance in text: KCNH2: Gly749Ala
PubMed Link: 33013630
Variant Present in the following documents:
  • Main text
  • fneur-11-00925.pdf
View BVdb publication page