p.Cys22 His23insArgValArgAlaAlaG variant of RARA (Retinoic acid receptor alpha)
p.Cys22 His23insArgValArgAlaAlaG in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
p.Cys22 His23insArgValArgAlaAlaG variant details
- gnomAD 17-40341435-A-AGC
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.185
- CADD 14.80
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available