R67S (p.Arg67Ser) variant of MAOB (P27338)
R67S (p.Arg67Ser) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
R67S (p.Arg67Ser) variant details
- p.Arg67Ser
- ExAC rs777268698
- TOPMed rs777268698
- gnomAD rs777268698
- Missense
- Variant Prioritization Score for Impact Estimate 0.667
- REVEL 0.77
- MetaLR 0.88
- MetaSVM 0.78
- CADD 24.00
- PolyPhen-2 0.85
- SIFT 0.02
- Most common in the Latino/Admixed American population (allele frequency 2.9e-05)
- Structural context available