SCN5A c.141C>A ;(p.P47=)

Variant ID: 3-38674658-G-T

NM_000335.4(SCN5A):c.141C>A;(p.P47=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genotype and Cardiac Outcomes in Pediatric Dilated Cardiomyopathy.

Journal Of The American Heart Association
Khan, Rabia S RS; Pahl, Elfriede E; Dellefave-Castillo, Lisa L; Rychlik, Karen K; Ing, Alexander A; Yap, Kai Lee KL; Brew, Casey C; Johnston, Jamie R JR; McNally, Elizabeth M EM; Webster, Gregory G
Publication Date: 2022-01-04

Variant appearance in text: SCN5A: 141C>A
PubMed Link: 34935411
Variant Present in the following documents:
  • JAH3-11-e022854.pdf
  • JAH3-11-e022854-s001.pdf
View BVdb publication page



Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families.

Genes
Zrzavy, Tobias T; Leutmezer, Fritz F; Kristoferitsch, Wolfgang W; Kornek, Barbara B; Schneider, Christine C; Rommer, Paulus P; Berger, Thomas T; Zimprich, Alexander A
Publication Date: 2020-08-25

Variant appearance in text: rs571894716
PubMed Link: 32854198
Variant Present in the following documents:
  • genes-11-00988-s001.pdf
View BVdb publication page