D17D (p.Asp17Asp) variant of PDE6B (P35913)
D17D (p.Asp17Asp) in PDE6B (P35913) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
D17D (p.Asp17Asp) variant details
- p.Asp17Asp
- gnomAD 4-625677-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.175
- CADD 1.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available