S138F (p.Ser138Phe) variant of RPGR (Q92834)
S138F (p.Ser138Phe) 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.
S138F (p.Ser138Phe) variant details
- p.Ser138Phe
- NCI-TCGA Cosmic COSV1001
- cosmic curated COSV10014
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available