M148V (p.Met148Val) variant of MAOB (P27338)
M148V (p.Met148Val) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
M148V (p.Met148Val) variant details
- p.Met148Val
- gnomAD rs1179798721
- Missense
- Variant Prioritization Score for Impact Estimate 0.309
- REVEL 0.28
- MetaLR 0.01
- MetaSVM -1.03
- CADD 17.60
- PolyPhen-2 0.02
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available