A19G (p.Ala19Gly) variant of MAOB (P27338)
A19G (p.Ala19Gly) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
A19G (p.Ala19Gly) variant details
- p.Ala19Gly
- ExAC rs773282941
- gnomAD rs773282941
- Missense
- Variant Prioritization Score for Impact Estimate 0.581
- REVEL 0.57
- MetaLR 0.29
- MetaSVM -0.15
- CADD 26.60
- PolyPhen-2 0.98
- SIFT 0.03
- Most common in the African/African-American population (allele frequency 3.8e-05)
- Structural context available