S39C (p.Ser39Cys) variant of CD3E (P07766)
S39C (p.Ser39Cys) in CD3E (P07766) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S39C (p.Ser39Cys) variant details
- p.Ser39Cys
- NCI-TCGA Cosmic COSV6234
- cosmic curated COSV62345
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available