W14R (p.Trp14Arg) variant of FLNB (Filamin-B)
W14R (p.Trp14Arg) in FLNB (Filamin-B) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
W14R (p.Trp14Arg) variant details
- p.Trp14Arg
- NCI-TCGA Cosmic COSV5588
- cosmic curated COSV55884
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- FLNB Filamin/ABP280 repeat-like domain domainome 1.0: score -0.746