D95N (p.Asp95Asn) variant of CNGA1 (P29973)
D95N (p.Asp95Asn) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
D95N (p.Asp95Asn) variant details
- p.Asp95Asn
- ExAC rs749149075
- gnomAD rs749149075
- Missense
- Variant Prioritization Score for Impact Estimate 0.316
- REVEL 0.11
- CADD 26.20
- PolyPhen-2 0.16
- SIFT 0.03
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available