E69K (p.Glu69Lys) variant of ANKRD1 (Q15327)
E69K (p.Glu69Lys) 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.
E69K (p.Glu69Lys) variant details
- p.Glu69Lys
- NCI-TCGA Cosmic COSV6331
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available