R11M (p.Arg11Met) variant of FHL1 (Q13642)
R11M (p.Arg11Met) in FHL1 (Q13642) 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.
R11M (p.Arg11Met) variant details
- p.Arg11Met
- NCI-TCGA Cosmic COSV6177
- cosmic curated COSV61779
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- FHL1 Zinc finger, LIM-type domain domainome 1.0: score -0.35