G33E (p.Gly33Glu) variant of SCN1B (Q07699)
G33E (p.Gly33Glu) in SCN1B (Q07699) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.96 / 1. The record also includes structural context.
G33E (p.Gly33Glu) variant details
- p.Gly33Glu
- NCI-TCGA Cosmic COSV9938
- cosmic curated COSV99386
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.961
- ESM-1b 1.00
- AlphaMissense 0.91
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available