F186L (p.Phe186Leu) variant of SCN5A (Q14524)
F186L (p.Phe186Leu) in SCN5A (Q14524) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F186L (p.Phe186Leu) variant details
- p.Phe186Leu
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10034
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available