S26F (p.Ser26Phe) variant of FSHR (P23945)
S26F (p.Ser26Phe) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
S26F (p.Ser26Phe) variant details
- p.Ser26Phe
- gnomAD rs1336784074
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- REVEL 0.42
- MetaLR 0.78
- MetaSVM 0.31
- CADD 22.00
- PolyPhen-2 0.03
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available