F26F (p.Phe26Phe) variant of RARA (Retinoic acid receptor alpha)
F26F (p.Phe26Phe) in RARA (Retinoic acid receptor alpha) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
F26F (p.Phe26Phe) variant details
- p.Phe26Phe
- rs746187167
- gnomAD 17-40331296-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.493
- CADD 11.80
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available
- Literature evidence available