C10Y (p.Cys10Tyr) variant of FHL1 (Q13642)
C10Y (p.Cys10Tyr) in FHL1 (Q13642) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Myopathy, reducing body, X-linked, childhood-onset; X-linked myopathy with postu. The available variant effect predictions contribute to a CATVariant prioritization score of 0.95 / 1. The record also includes experimental measurements, published literature, and structural context.
C10Y (p.Cys10Tyr) variant details
- p.Cys10Tyr
- rs2148371537
- ClinGen CA414607428
- ClinVar RCV001921309
- ClinVar RCV002441046
- Uncertain significance
- Myopathy, reducing body, X-linked, childhood-onset; X-linked myopathy with postu
- Missense
- Variant Prioritization Score for Impact Estimate 0.953
- AlphaMissense 1.00
- MetaLR 1.00
- MetaSVM 0.91
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.83
- ClinVar: Uncertain significance (Myopathy, reducing body, X-linked, childhood-onset; X-linked myo)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- FHL1 Zinc finger, LIM-type domain domainome 1.0: score -0.176
- Cited in: Emery-Dreifuss Muscular Dystrophy. (PMID 20301609)
- Cited in: 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and… (PMID 25173338)