D42H (p.Asp42His) variant of SOS1 (Son of sevenless homolog 1)
D42H (p.Asp42His) 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.
D42H (p.Asp42His) variant details
- p.Asp42His
- NCI-TCGA Cosmic COSV6767
- cosmic curated COSV67675
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available