L39F (p.Leu39Phe) variant of SCN1B (Q07699)
L39F (p.Leu39Phe) in SCN1B (Q07699) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes structural context.
L39F (p.Leu39Phe) variant details
- p.Leu39Phe
- gnomAD rs1395531462
- Missense
- Variant Prioritization Score for Impact Estimate 0.222
- ESM-1b 0.00
- AlphaMissense 0.55
- Structural context available