SCN5A c.5531G>C ;(p.G1844A)

Variant ID: 3-38592329-C-G

NM_000335.4(SCN5A):c.5531G>C;(p.G1844A)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea.

Journal Of Korean Medical Science
Son, Min-Jeong MJ; Kim, Min-Kyoung MK; Yang, Kyung-Moo KM; Choi, Byung-Ha BH; Lee, Bong Woo BW; Yoo, Seong Ho SH
Publication Date: 2018-08-06

Variant appearance in text: SCN5A: g1844a
PubMed Link: 30079003
Variant Present in the following documents:
  • jkms-33-e200.pdf
View BVdb publication page



Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young.

Genome Research
Methner, D Nicole R DN; Scherer, Steven E SE; Welch, Katherine K; Walkiewicz, Magdalena M; Eng, Christine M CM; Belmont, John W JW; Powell, Mark C MC; Korchina, Viktoriya V; Doddapaneni, Harsha Vardhan HV; Muzny, Donna M DM; Gibbs, Richard A RA; Wolf, Dwayne A DA; Sanchez, Luis A LA; Kahn, Roger R
Publication Date: 2016-09

Variant appearance in text: SCN5A: G1844A
PubMed Link: 27435932
Variant Present in the following documents:
  • 1170.pdf
View BVdb publication page



The genetics of pro-arrhythmic adverse drug reactions.

British Journal Of Clinical Pharmacology
Petropoulou, Evmorfia E; Jamshidi, Yalda Y; Behr, Elijah R ER
Publication Date: 2014-04

Variant appearance in text: SCN5A: G1844A
PubMed Link: 23834499
Variant Present in the following documents:
  • Main text
View BVdb publication page