F162V (p.Phe162Val) variant of RPGR (Q92834)
F162V (p.Phe162Val) in RPGR (Q92834) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F162V (p.Phe162Val) variant details
- p.Phe162Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available