R69L (p.Arg69Leu) variant of FLNB (Filamin-B)
R69L (p.Arg69Leu) 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.
R69L (p.Arg69Leu) variant details
- p.Arg69Leu
- NCI-TCGA Cosmic COSV9991
- cosmic curated COSV99913
- 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 -0.194