P38S (p.Pro38Ser) variant of SOST (Sclerostin)
P38S (p.Pro38Ser) in SOST (Sclerostin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- ESP rs373660644
- ExAC rs373660644
- TOPMed rs373660644
- gnomAD rs373660644
- Missense
- Variant Prioritization Score for Impact Estimate 0.564
- REVEL 0.43
- CADD 24.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available