M122V (p.Met122Val) variant of MAOB (P27338)
M122V (p.Met122Val) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
M122V (p.Met122Val) variant details
- p.Met122Val
- TOPMed rs2034619785
- Missense
- Variant Prioritization Score for Impact Estimate 0.276
- REVEL 0.29
- MetaLR 0.61
- MetaSVM -0.11
- CADD 5.61
- PolyPhen-2 0.01
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available