A13D (p.Ala13Asp) variant of RPGR (Q92834)
A13D (p.Ala13Asp) 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.
A13D (p.Ala13Asp) variant details
- p.Ala13Asp
- NCI-TCGA Cosmic COSV5883
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available