R197S (p.Arg197Ser) variant of MAOB (P27338)
R197S (p.Arg197Ser) 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.
R197S (p.Arg197Ser) variant details
- p.Arg197Ser
- Ensembl rs12845783
- Missense
- Variant Prioritization Score for Impact Estimate 0.583
- REVEL 0.68
- MetaLR 0.78
- MetaSVM 0.35
- CADD 23.80
- PolyPhen-2 0.99
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available