SCN5A c.446C>A ;(p.A149D)

Variant ID: 3-38663927-G-T

NM_000335.4(SCN5A):c.446C>A;(p.A149D)

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:

Rare Association of two Genetic Causes of Sudden Death in a Young Survivor.

Arquivos Brasileiros De Cardiologia
Brito, Dulce D; Magalhães, Andreia A; Cortez-Dias, Nuno N; Miltenberger-Miltenyi, Gabriel G
Publication Date: 2017-02

Variant appearance in text: SCN5A: 446C>A
PubMed Link: 28327871
Variant Present in the following documents:
  • Main text
  • abc-108-02-0184.pdf
View BVdb publication page