Q79P (p.Gln79Pro) variant of FSHR (P23945)
Q79P (p.Gln79Pro) 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.
Q79P (p.Gln79Pro) variant details
- p.Gln79Pro
- NCI-TCGA Cosmic COSV5862
- cosmic curated COSV58620
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available