G71R (p.Gly71Arg) variant of CNGA1 (P29973)
G71R (p.Gly71Arg) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
G71R (p.Gly71Arg) variant details
- p.Gly71Arg
- 1000Genomes rs186611254
- ExAC rs186611254
- gnomAD rs186611254
- Missense
- Variant Prioritization Score for Impact Estimate 0.173
- REVEL 0.05
- CADD 10.90
- PolyPhen-2 0.11
- SIFT 0.16
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available