R87G (p.Arg87Gly) variant of MAOB (P27338)
R87G (p.Arg87Gly) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
R87G (p.Arg87Gly) variant details
- p.Arg87Gly
- 1000Genomes rs776880004
- TOPMed rs776880004
- gnomAD rs776880004
- Missense
- Variant Prioritization Score for Impact Estimate 0.457
- REVEL 0.40
- MetaLR 0.70
- MetaSVM 0.40
- CADD 12.50
- PolyPhen-2 0.16
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available