F168L (p.Phe168Leu) variant of MAOB (P27338)
F168L (p.Phe168Leu) in MAOB (P27338) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
F168L (p.Phe168Leu) variant details
- p.Phe168Leu
- NCI-TCGA Cosmic COSV6520
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.633
- REVEL 0.75
- MetaLR 0.63
- MetaSVM 0.06
- CADD 21.70
- PolyPhen-2 0.09
- SIFT 0.04
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 3.8e-05)
- Structural context available