Q96E (p.Gln96Glu) variant of CNGA1 (P29973)
Q96E (p.Gln96Glu) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
Q96E (p.Gln96Glu) variant details
- p.Gln96Glu
- TOPMed rs1560624914
- gnomAD rs1560624914
- Missense
- Variant Prioritization Score for Impact Estimate 0.216
- REVEL 0.04
- CADD 19.20
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available