R59G (p.Arg59Gly) variant of FHL1 (Q13642)
R59G (p.Arg59Gly) 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.
R59G (p.Arg59Gly) variant details
- p.Arg59Gly
- NCI-TCGA TCGA novel
- 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 -0.0049