P38P (p.Pro38Pro) variant of RARA (Retinoic acid receptor alpha)
P38P (p.Pro38Pro) in RARA (Retinoic acid receptor alpha) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
P38P (p.Pro38Pro) variant details
- p.Pro38Pro
- rs1232082912
- gnomAD 17-40331332-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.102
- CADD 2.95
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available