F27F (p.Phe27Phe) variant of RARA (Retinoic acid receptor alpha)
F27F (p.Phe27Phe) 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.
F27F (p.Phe27Phe) variant details
- p.Phe27Phe
- rs2033684316
- gnomAD 17-40331299-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.492
- CADD 11.90
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available