V39F (p.Val39Phe) variant of FERMT1 (Fermitin family homolog 1)
V39F (p.Val39Phe) in FERMT1 (Fermitin family homolog 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V39F (p.Val39Phe) variant details
- p.Val39Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available