D89A (p.Asp89Ala) variant of SOS1 (Son of sevenless homolog 1)
D89A (p.Asp89Ala) 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.
D89A (p.Asp89Ala) variant details
- p.Asp89Ala
- NCI-TCGA Cosmic COSV1012
- cosmic curated COSV10121
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available