D38D (p.Asp38Asp) variant of PDE6B (P35913)
D38D (p.Asp38Asp) in PDE6B (P35913) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
D38D (p.Asp38Asp) variant details
- p.Asp38Asp
- rs371572108
- gnomAD 4-625740-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.081
- CADD 0.05
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available