F22S (p.Phe22Ser) variant of FLNB (Filamin-B)
F22S (p.Phe22Ser) in FLNB (Filamin-B) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes experimental measurements and structural context.
F22S (p.Phe22Ser) variant details
- p.Phe22Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available
- FLNB Filamin/ABP280 repeat-like domain domainome 1.0: score -0.923