N89Y (p.Asn89Tyr) variant of CNGA1 (P29973)
N89Y (p.Asn89Tyr) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
N89Y (p.Asn89Tyr) variant details
- p.Asn89Tyr
- gnomAD rs1284059893
- Missense
- Variant Prioritization Score for Impact Estimate 0.36
- REVEL 0.15
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.19
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available