SCN5A c.1427G>T ;(p.S476I)

Variant ID: 3-38646311-C-A

NM_000335.4(SCN5A):c.1427G>T;(p.S476I)

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:

A rare loss-of-function SCN5A variant is associated with lidocaine-induced ventricular fibrillation.

The Pharmacogenomics Journal
Xiong, Q Q; Cao, L L; Hu, J J; Marian, A J AJ; Hong, K K
Publication Date: 2014-08

Variant appearance in text: SCN5A: 1427G>T
PubMed Link: 24445991
Variant Present in the following documents:
  • Main text
  • nihms547860.pdf
View BVdb publication page