P29H (p.Pro29His) variant of RARA (Retinoic acid receptor alpha)
P29H (p.Pro29His) in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
P29H (p.Pro29His) variant details
- p.Pro29His
- TOPMed rs1297897531
- gnomAD rs1297897531
- Missense
- Variant Prioritization Score for Impact Estimate 0.673
- REVEL 0.59
- CADD 25.50
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available