G19R (p.Gly19Arg) variant of PRPH2 (Peripherin-2)
G19R (p.Gly19Arg) in PRPH2 (Peripherin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G19R (p.Gly19Arg) variant details
- p.Gly19Arg
- NCI-TCGA Cosmic COSV5783
- TOPMed rs1761919919
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available