C1914Y (p.Cys1914Tyr) variant of FBN1 (Fibrillin-1)
C1914Y (p.Cys1914Tyr) in FBN1 (Fibrillin-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Familial thoracic aortic aneurysm and aortic dissection; Marfan syndrome. The record also includes variant effect predictions and published literature.
C1914Y (p.Cys1914Tyr) variant details
- p.Cys1914Tyr
- rs1555395827
- ClinGen CA392341202
- ClinVar RCV002294598
- ClinVar RCV002346577
- Likely pathogenic
- Familial thoracic aortic aneurysm and aortic dissection; Marfan syndrome
- Missense
- MutPred 1.00
- ClinVar: Likely pathogenic (Familial thoracic aortic aneurysm and aortic dissection; Marfan)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Cited in: Heritable Thoracic Aortic Disease Overview. (PMID 20301299)
- Cited in: Canadian Cardiovascular Society position statement on the management of thoracic aortic disease. (PMID 24882528)