I23V (p.Ile23Val) variant of CNGA1 (P29973)
I23V (p.Ile23Val) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
I23V (p.Ile23Val) variant details
- p.Ile23Val
- gnomAD rs1398996857
- Missense
- Variant Prioritization Score for Impact Estimate 0.178
- REVEL 0.03
- CADD 15.80
- PolyPhen-2 0.00
- SIFT 0.73
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available