G76R (p.Gly76Arg) variant of MAOB (P27338)
G76R (p.Gly76Arg) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data and structural context.
G76R (p.Gly76Arg) variant details
- p.Gly76Arg
- Ensembl rs2035101065
- Missense
- Variant Prioritization Score for Impact Estimate 0.538
- REVEL 0.58
- MetaLR 0.22
- MetaSVM -0.44
- CADD 24.50
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available