F17I (p.Phe17Ile) variant of SCN2A (Q99250)
F17I (p.Phe17Ile) in SCN2A (Q99250) 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 0.93 / 1. The record also includes structural context.
F17I (p.Phe17Ile) variant details
- p.Phe17Ile
- NCI-TCGA Cosmic COSV5185
- cosmic curated COSV51850
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.925
- ESM-1b 1.00
- AlphaMissense 0.84
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available