S77K (p.Ser77Lys) variant of SOS1 (Son of sevenless homolog 1)
S77K (p.Ser77Lys) in SOS1 (Son of sevenless homolog 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S77K (p.Ser77Lys) variant details
- p.Ser77Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available