KCNQ1 c.1437C>G ;(p.F479L)

Variant ID: 11-2683234-C-G

NM_000218.2(KCNQ1):c.1437C>G;(p.F479L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benign.

Heart Rhythm
Clemens, Daniel J DJ; Lentino, Anne R AR; Kapplinger, Jamie D JD; Ye, Dan D; Zhou, Wei W; Tester, David J DJ; Ackerman, Michael J MJ
Publication Date: 2018-04

Variant appearance in text: KCNQ1: F479L
PubMed Link: 29197658
Variant Present in the following documents:
  • Main text
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