C10F (p.Cys10Phe) variant of FHL1 (Q13642)
C10F (p.Cys10Phe) 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.
C10F (p.Cys10Phe) variant details
- p.Cys10Phe
- cosmic curated COSV10886
- 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 -0.176