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SCN5A c.1018C>G ;(p.R340G)
Variant ID: 3-38648282-G-C
NM_000335.4(
SCN5A
):c.1018C>G;(p.R340G)
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:
Atrial fibrillation: the role of common and rare genetic variants.
European Journal Of Human Genetics : Ejhg
Olesen, Morten S MS; Nielsen, Morten W MW; Haunsø, Stig S; Svendsen, Jesper H JH
Publication Date: 2014-03
Variant appearance in text: SCN5A: 1018C>G
PubMed Link:
23838598
Variant Present in the following documents:
Main text
View BVdb publication page