G38V (p.Gly38Val) variant of FKRP (Q9H9S5)
G38V (p.Gly38Val) in FKRP (Q9H9S5) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G38V (p.Gly38Val) variant details
- p.Gly38Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available