F62S (p.Phe62Ser) variant of CNGA1 (P29973)
F62S (p.Phe62Ser) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
F62S (p.Phe62Ser) variant details
- p.Phe62Ser
- Ensembl rs1578076849
- Missense
- Variant Prioritization Score for Impact Estimate 0.0485
- REVEL 0.01
- CADD 3.16
- PolyPhen-2 0.00
- SIFT 0.79
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available