G16V (p.Gly16Val) variant of CHEK1 (O14757)
G16V (p.Gly16Val) 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.
G16V (p.Gly16Val) variant details
- p.Gly16Val
- NCI-TCGA Cosmic COSV9962
- cosmic curated COSV99629
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available