L91F (p.Leu91Phe) variant of NOS1AP (O75052)
L91F (p.Leu91Phe) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
L91F (p.Leu91Phe) variant details
- p.Leu91Phe
- TOPMed rs1261184608
- gnomAD rs1261184608
- Missense
- Variant Prioritization Score for Impact Estimate 0.175
- REVEL 0.04
- CADD 18.20
- PolyPhen-2 0.01
- SIFT 0.71
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available