S55L (p.Ser55Leu) variant of LHCGR (P22888)
S55L (p.Ser55Leu) in LHCGR (P22888) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S55L (p.Ser55Leu) variant details
- p.Ser55Leu
- NCI-TCGA Cosmic COSV9968
- cosmic curated COSV99683
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available