G56A (p.Gly56Ala) variant of CYP27B1 (O15528)
G56A (p.Gly56Ala) in CYP27B1 (O15528) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
G56A (p.Gly56Ala) variant details
- p.Gly56Ala
- ExAC rs769363080
- TOPMed rs769363080
- gnomAD rs769363080
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.262
- ESM-1b 0.00
- AlphaMissense 0.16
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available