L92F (p.Leu92Phe) variant of NOS1AP (O75052)
L92F (p.Leu92Phe) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
L92F (p.Leu92Phe) variant details
- p.Leu92Phe
- TOPMed rs1442779059
- gnomAD rs1442779059
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.14
- CADD 22.30
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available