R41G (p.Arg41Gly) variant of SCN4A (Nav1.4)
R41G (p.Arg41Gly) in SCN4A (Nav1.4) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R41G (p.Arg41Gly) variant details
- p.Arg41Gly
- NCI-TCGA Cosmic COSV1014
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available