G41V (p.Gly41Val) variant of G6PD (P11413)
G41V (p.Gly41Val) in G6PD (P11413) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G41V (p.Gly41Val) variant details
- p.Gly41Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available