I6N (p.Ile6Asn) variant of CNGA1 (P29973)
I6N (p.Ile6Asn) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
I6N (p.Ile6Asn) variant details
- p.Ile6Asn
- ExAC rs760929254
- gnomAD rs760929254
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- REVEL 0.10
- CADD 24.40
- PolyPhen-2 0.35
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available