F139V (p.Phe139Val) variant of ANKRD1 (Q15327)
F139V (p.Phe139Val) 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.
F139V (p.Phe139Val) variant details
- p.Phe139Val
- NCI-TCGA Cosmic COSV6331
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available