Bibliome.ai browser hg19
Search
About
Stats
FAQ
SCN5A c.367G>A ;(p.A123T)
Variant ID: 3-38671827-C-T
NM_000335.4(
SCN5A
):c.367G>A;(p.A123T)
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:
Cytoskeletal Protein Variants Driving Atrial Fibrillation: Potential Mechanisms of Action.
Cells
van Wijk, Stan W SW; Su, Wei W; Wijdeveld, Leonoor F J M LFJM; Ramos, Kennedy S KS; Brundel, Bianca J J M BJJM
Publication Date: 2022-01-25
Variant appearance in text: SCN5A: A123T
PubMed Link:
35159226
Variant Present in the following documents:
Main text
cells-11-00416.pdf
View BVdb publication page
Cytoskeletal Protein Variants Driving Atrial Fibrillation: Potential Mechanisms of Action.
Cells
van Wijk, Stan W SW; Su, Wei W; Wijdeveld, Leonoor F J M LFJM; Ramos, Kennedy S KS; Brundel, Bianca J J M BJJM
Publication Date: 2022-01-25
Variant appearance in text: SCN5A: A123T
PubMed Link:
35159226
Variant Present in the following documents:
Main text
cells-11-00416.pdf
View BVdb publication page