F78I (p.Phe78Ile) variant of SOS1 (Son of sevenless homolog 1)
F78I (p.Phe78Ile) in SOS1 (Son of sevenless homolog 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F78I (p.Phe78Ile) variant details
- p.Phe78Ile
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available