G16C (p.Gly16Cys) variant of ANKRD1 (Q15327)
G16C (p.Gly16Cys) in ANKRD1 (Q15327) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G16C (p.Gly16Cys) variant details
- p.Gly16Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available