R39G (p.Arg39Gly) variant of USH2A (Usherin)
R39G (p.Arg39Gly) in USH2A (Usherin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R39G (p.Arg39Gly) variant details
- p.Arg39Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available