SCN5A c.3319_3321delinsATG ;(p.A1107M)

Variant ID: 3-38620891-GGC-CAT

NM_000335.4(SCN5A):c.3319_3321delinsATG;(p.A1107M)

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:

"Ryanopathies" and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?

Cell Death & Disease
Sleiman, Yvonne Y; Lacampagne, Alain A; Meli, Albano C AC
Publication Date: 2021-11-01

Variant appearance in text: SCN5A: A1107M
PubMed Link: 34725342
Variant Present in the following documents:
  • Main text
  • 41419_2021_Article_4337.pdf
View BVdb publication page


"Ryanopathies" and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?

Cell Death & Disease
Sleiman, Yvonne Y; Lacampagne, Alain A; Meli, Albano C AC
Publication Date: 2021-11-01

Variant appearance in text: SCN5A: A1107M
PubMed Link: 34725342
Variant Present in the following documents:
  • Main text
  • 41419_2021_Article_4337.pdf
View BVdb publication page