N17K (p.Asn17Lys) variant of RARA (Retinoic acid receptor alpha)
N17K (p.Asn17Lys) in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
N17K (p.Asn17Lys) variant details
- p.Asn17Lys
- rs972734651
- gnomAD 17-40341473-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- CADD 13.00
- Most common in the African/African-American population (allele frequency 7.2e-05)
- Structural context available
- Literature evidence available