C21C (p.Cys21Cys) variant of SCN1B (Q07699)
C21C (p.Cys21Cys) 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.
C21C (p.Cys21Cys) variant details
- p.Cys21Cys
- rs200339565
- gnomAD 19-35032550-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.102
- CADD 2.95
- Most common in the Non-Finnish European population (allele frequency 5.9e-05)
- Structural context available
- Literature evidence available