G39G (p.Gly39Gly) variant of PDE6B (P35913)
G39G (p.Gly39Gly) 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.
G39G (p.Gly39Gly) variant details
- p.Gly39Gly
- rs140538420
- gnomAD 4-625743-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.082
- CADD 0.19
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available