S3N (p.Ser3Asn) variant of RARA (Retinoic acid receptor alpha)
S3N (p.Ser3Asn) in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
S3N (p.Ser3Asn) variant details
- p.Ser3Asn
- gnomAD rs1403940287
- Missense
- Variant Prioritization Score for Impact Estimate 0.545
- REVEL 0.41
- CADD 23.60
- PolyPhen-2 0.05
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available