P138R (p.Pro138Arg) variant of MAOB (P27338)
P138R (p.Pro138Arg) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
P138R (p.Pro138Arg) variant details
- p.Pro138Arg
- TOPMed rs2034603615
- Missense
- Variant Prioritization Score for Impact Estimate 0.774
- REVEL 0.88
- MetaLR 0.83
- MetaSVM 0.78
- CADD 23.60
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available