P47Q (p.Pro47Gln) variant of SOST (Sclerostin)
P47Q (p.Pro47Gln) in SOST (Sclerostin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
P47Q (p.Pro47Gln) variant details
- p.Pro47Gln
- TOPMed rs1428033627
- gnomAD rs1428033627
- Missense
- Variant Prioritization Score for Impact Estimate 0.301
- REVEL 0.30
- CADD 20.60
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available