N93S (p.Asn93Ser) variant of CNGA1 (P29973)
N93S (p.Asn93Ser) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
N93S (p.Asn93Ser) variant details
- p.Asn93Ser
- Ensembl rs1055857820
- Missense
- Variant Prioritization Score for Impact Estimate 0.331
- REVEL 0.11
- CADD 23.90
- PolyPhen-2 0.97
- SIFT 0.26
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available