S91N (p.Ser91Asn) variant of CNGA1 (P29973)
S91N (p.Ser91Asn) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
S91N (p.Ser91Asn) variant details
- p.Ser91Asn
- ExAC rs778736952
- gnomAD rs778736952
- Missense
- Variant Prioritization Score for Impact Estimate 0.347
- REVEL 0.04
- CADD 23.30
- PolyPhen-2 0.52
- SIFT 0.39
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available