S36P (p.Ser36Pro) variant of RARA (Retinoic acid receptor alpha)
S36P (p.Ser36Pro) in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
S36P (p.Ser36Pro) variant details
- p.Ser36Pro
- gnomAD 17-40341504-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.122
- CADD 5.78
- Most common in the Non-Finnish European population (allele frequency 9.5e-07)
- Structural context available
- Literature evidence available