L155F (p.Leu155Phe) variant of MAOB (P27338)
L155F (p.Leu155Phe) in MAOB (P27338) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
L155F (p.Leu155Phe) variant details
- p.Leu155Phe
- rs201889071
- ClinGen CA10391277
- ClinVar RCV004291306
- 1000Genomes rs201889071
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.201
- REVEL 0.22
- MetaLR 0.49
- MetaSVM -0.55
- CADD 3.14
- PolyPhen-2 0.08
- SIFT 0.05
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the 1KG:CHS population (allele frequency 0.0065)
- Structural context available