V22V (p.Val22Val) variant of SCN1B (Q07699)
V22V (p.Val22Val) in SCN1B (Q07699) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
V22V (p.Val22Val) variant details
- p.Val22Val
- rs769410262
- gnomAD 19-35032553-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.491
- CADD 12.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 7.5e-05)
- Structural context available
- Literature evidence available