G17E (p.Gly17Glu) variant of FSHR (P23945)
G17E (p.Gly17Glu) in FSHR (P23945) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G17E (p.Gly17Glu) variant details
- p.Gly17Glu
- NCI-TCGA Cosmic COSV5862
- cosmic curated COSV58623
- NCI-TCGA Cosmic COSV5863
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available