D71G (p.Asp71Gly) variant of FSHR (P23945)
D71G (p.Asp71Gly) in FSHR (P23945) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
D71G (p.Asp71Gly) variant details
- p.Asp71Gly
- NCI-TCGA Cosmic COSV5862
- cosmic curated COSV58621
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.45
- MetaSVM -0.25
- SIFT 0.32
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available