SCN5A c.1937A>G ;(p.Q646R)

Variant ID: 3-38640495-T-C

NM_000335.4(SCN5A):c.1937A>G;(p.Q646R)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.

Circulation
Kanter, Ronald J RJ; Pfeiffer, Ryan R; Hu, Dan D; Barajas-Martinez, Héctor H; Carboni, Michael P MP; Antzelevitch, Charles C
Publication Date: 2012-01-03

Variant appearance in text: SCN5A: Q646R
PubMed Link: 22090166
Variant Present in the following documents:
  • Main text
View BVdb publication page