N55D (p.Asn55Asp) variant of CNGA1 (P29973)
N55D (p.Asn55Asp) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
N55D (p.Asn55Asp) variant details
- p.Asn55Asp
- Ensembl rs2110157829
- Missense
- Variant Prioritization Score for Impact Estimate 0.129
- REVEL 0.05
- CADD 10.10
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available