D227G (p.Asp227Gly) variant of MAOB (P27338)
D227G (p.Asp227Gly) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
D227G (p.Asp227Gly) variant details
- p.Asp227Gly
- TOPMed rs2034520809
- gnomAD rs2034520809
- Missense
- Variant Prioritization Score for Impact Estimate 0.412
- REVEL 0.32
- MetaLR 0.50
- MetaSVM -0.35
- CADD 21.00
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available