G19G (p.Gly19Gly) variant of SCN1B (Q07699)
G19G (p.Gly19Gly) in SCN1B (Q07699) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
G19G (p.Gly19Gly) variant details
- p.Gly19Gly
- gnomAD 19-35032544-G-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.303
- CADD 9.26
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available