SCN5A c.1582A>T ;(p.S528C)

Variant ID: 3-38645511-T-A

NM_000335.4(SCN5A):c.1582A>T;(p.S528C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.

Journal Of The American College Of Cardiology
Nademanee, Koonlawee K; Raju, Hariharan H; de Noronha, Sofia V SV; Papadakis, Michael M; Robinson, Laurence L; Rothery, Stephen S; Makita, Naomasa N; Kowase, Shinya S; Boonmee, Nakorn N; Vitayakritsirikul, Vorapot V; Ratanarapee, Samrerng S; Sharma, Sanjay S; van der Wal, Allard C AC; Christiansen, Michael M; Tan, Hanno L HL; Wilde, Arthur A AA; Nogami, Akihiko A; Sheppard, Mary N MN; Veerakul, Gumpanart G; Behr, Elijah R ER
Publication Date: 2015-11-03

Variant appearance in text: SCN5A: Ser528Cys
PubMed Link: 26516000
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page