R38G (p.Arg38Gly) variant of SCN4A (Nav1.4)
R38G (p.Arg38Gly) in SCN4A (Nav1.4) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R38G (p.Arg38Gly) variant details
- p.Arg38Gly
- ExAC rs776201356
- TOPMed rs776201356
- gnomAD rs776201356
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available