R68G (p.Arg68Gly) variant of CNGA1 (P29973)
R68G (p.Arg68Gly) 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.
R68G (p.Arg68Gly) variant details
- p.Arg68Gly
- TOPMed rs1317730341
- gnomAD rs1317730341
- Missense
- Variant Prioritization Score for Impact Estimate 0.0544
- REVEL 0.02
- CADD 5.67
- PolyPhen-2 0.00
- SIFT 0.35
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available