I49N (p.Ile49Asn) variant of FSHR (P23945)
I49N (p.Ile49Asn) 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.
I49N (p.Ile49Asn) variant details
- p.Ile49Asn
- NCI-TCGA Cosmic COSV5863
- cosmic curated COSV58634
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available