A62T (p.Ala62Thr) variant of SOS2 (Son of sevenless homolog 2)
A62T (p.Ala62Thr) 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 structural context.
A62T (p.Ala62Thr) variant details
- p.Ala62Thr
- NCI-TCGA Cosmic COSV9936
- cosmic curated COSV99365
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available