SCN5A c.1120T>C ;(p.W374R)

Variant ID: 3-38648180-A-G

NM_000335.4(SCN5A):c.1120T>C;(p.W374R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes.

Ebiomedicine
Campuzano, Oscar O; Sarquella-Brugada, Georgia G; Fernandez-Falgueras, Anna A; Coll, Mónica M; Iglesias, Anna A; Ferrer-Costa, Carles C; Cesar, Sergi S; Arbelo, Elena E; García-Álvarez, Ana A; Jordà, Paloma P; Toro, Rocío R; Tiron de Llano, Coloma C; Grassi, Simone S; Oliva, Antonio A; Brugada, Josep J; Brugada, Ramon R
Publication Date: 2020-04

Variant appearance in text: SCN5A: 1120T>C; Trp374Arg
PubMed Link: 32268277
Variant Present in the following documents:
  • Main text
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