W107R (p.Trp107Arg) variant of MAOB (P27338)
W107R (p.Trp107Arg) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
W107R (p.Trp107Arg) variant details
- p.Trp107Arg
- ExAC rs774521579
- TOPMed rs774521579
- gnomAD rs774521579
- Missense
- Variant Prioritization Score for Impact Estimate 0.47
- REVEL 0.56
- MetaLR 0.64
- MetaSVM -0.02
- CADD 17.00
- PolyPhen-2 0.03
- SIFT 0.08
- Most common in the Latino/Admixed American population (allele frequency 3.8e-05)
- Structural context available