G10V (p.Gly10Val) variant of SCN1A (P35498)
G10V (p.Gly10Val) in SCN1A (P35498) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G10V (p.Gly10Val) variant details
- p.Gly10Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available