S26S (p.Ser26Ser) variant of SCN1B (Q07699)
S26S (p.Ser26Ser) in SCN1B (Q07699) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
S26S (p.Ser26Ser) variant details
- p.Ser26Ser
- rs774401364
- gnomAD 19-35032565-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.104
- CADD 3.35
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available