Y97H (p.Tyr97His) variant of MAOB (P27338)
Y97H (p.Tyr97His) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
Y97H (p.Tyr97His) variant details
- p.Tyr97His
- TOPMed rs1215586148
- gnomAD rs1215586148
- Missense
- Variant Prioritization Score for Impact Estimate 0.358
- REVEL 0.31
- MetaLR 0.56
- MetaSVM -0.20
- CADD 22.10
- PolyPhen-2 0.03
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available