T10N (p.Thr10Asn) variant of RARA (Retinoic acid receptor alpha)
T10N (p.Thr10Asn) in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
T10N (p.Thr10Asn) variant details
- p.Thr10Asn
- gnomAD 17-40341460-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.389
- CADD 18.10
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available
- Literature evidence available