P56T (p.Pro56Thr) variant of CNGA1 (P29973)
P56T (p.Pro56Thr) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
P56T (p.Pro56Thr) variant details
- p.Pro56Thr
- 1000Genomes rs200810027
- ExAC rs200810027
- gnomAD rs200810027
- Missense
- Variant Prioritization Score for Impact Estimate 0.0614
- REVEL 0.04
- CADD 0.56
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available