G39G (p.Gly39Gly) variant of RARA (Retinoic acid receptor alpha)
G39G (p.Gly39Gly) in RARA (Retinoic acid receptor alpha) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
G39G (p.Gly39Gly) variant details
- p.Gly39Gly
- rs767135725
- gnomAD 17-40331335-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.16
- CADD 8.68
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available
- Literature evidence available