SCN5A c.3248G>A ;(p.G1083D)

Variant ID: 3-38620964-C-T

NM_000335.4(SCN5A):c.3248G>A;(p.G1083D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.

Journal Of The American College Of Cardiology
Lahrouchi, Najim N; Raju, Hariharan H; Lodder, Elisabeth M EM; Papatheodorou, Efstathios E; Ware, James S JS; Papadakis, Michael M; Tadros, Rafik R; Cole, Della D; Skinner, Jonathan R JR; Crawford, Jackie J; Love, Donald R DR; Pua, Chee J CJ; Soh, Bee Y BY; Bhalshankar, Jaydutt D JD; Govind, Risha R; Tfelt-Hansen, Jacob J; Winkel, Bo G BG; van der Werf, Christian C; Wijeyeratne, Yanushi D YD; Mellor, Greg G; Till, Jan J; Cohen, Marta C MC; Tome-Esteban, Maria M; Sharma, Sanjay S; Wilde, Arthur A M AAM; Cook, Stuart A SA; Bezzina, Connie R CR; Sheppard, Mary N MN; Behr, Elijah R ER
Publication Date: 2017-05-02

Variant appearance in text: SCN5A: G1083D
PubMed Link: 28449774
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page