L91I (p.Leu91Ile) variant of NOS1AP (O75052)
L91I (p.Leu91Ile) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
L91I (p.Leu91Ile) variant details
- p.Leu91Ile
- TOPMed rs1261184608
- gnomAD rs1261184608
- Missense
- Variant Prioritization Score for Impact Estimate 0.16
- REVEL 0.02
- CADD 16.60
- PolyPhen-2 0.10
- SIFT 0.42
- Most common in the East Asian population (allele frequency 0.00039)
- Structural context available