SCN5A c.668T>G ;(p.V223G)

Variant ID: 3-38655269-A-C

NM_000335.4(SCN5A):c.668T>G;(p.V223G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: SCN5A: Val223Gly
PubMed Link: 33013630
Variant Present in the following documents:
  • Main text
  • fneur-11-00925.pdf
View BVdb publication page



Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia-Related Genes.

Journal Of The American Heart Association
Chahal, C Anwar A CAA; Salloum, Mohammad N MN; Alahdab, Fares F; Gottwald, Joseph A JA; Tester, David J DJ; Anwer, Lucman A LA; So, Elson L EL; Murad, Mohammad Hassan MH; St Louis, Erik K EK; Ackerman, Michael J MJ; Somers, Virend K VK
Publication Date: 2020-01-07

Variant appearance in text: SCN5A: Val223Gly
PubMed Link: 31865891
Variant Present in the following documents:
  • JAH3-9-e012264.pdf
  • JAH3-9-e012264-s001.pdf
View BVdb publication page