N17D (p.Asn17Asp) variant of RARA (Retinoic acid receptor alpha)
N17D (p.Asn17Asp) in RARA (Retinoic acid receptor alpha) 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, published literature, and structural context.
N17D (p.Asn17Asp) variant details
- p.Asn17Asp
- gnomAD 17-40341471-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.326
- CADD 12.40
- Population evidence available
- Structural context available
- Literature evidence available