G13D (p.Gly13Asp) variant of FLNC (Filamin-C)
G13D (p.Gly13Asp) in FLNC (Filamin-C) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G13D (p.Gly13Asp) variant details
- p.Gly13Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available