F11C (p.Phe11Cys) variant of SOS2 (Son of sevenless homolog 2)
F11C (p.Phe11Cys) in SOS2 (Son of sevenless homolog 2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
F11C (p.Phe11Cys) variant details
- p.Phe11Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.49
- MetaSVM -0.20
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available