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SCN5A c.706_708delinsATC ;(p.L236I)
Variant ID: 3-38651451-CAG-GAT
NM_000335.4(
SCN5A
):c.706_708delinsATC;(p.L236I)
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:
Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.
Biomedical Reports
Golubenko, Maria M; Mikhailov, Vadim V; Rusinova, Valeria V; Shestak, Anna A; Zaklyazminskaya, Elena E
Publication Date: 2020-09
Variant appearance in text: SCN5A: Leu236Ile
PubMed Link:
32765855
Variant Present in the following documents:
Main text
View BVdb publication page