E32D (p.Glu32Asp) variant of CHEK1 (O14757)
E32D (p.Glu32Asp) in CHEK1 (O14757) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E32D (p.Glu32Asp) variant details
- p.Glu32Asp
- NCI-TCGA Cosmic COSV5402
- cosmic curated COSV54022
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available