N98S (p.Asn98Ser) variant of FBN1 (Fibrillin-1)
N98S (p.Asn98Ser) in FBN1 (Fibrillin-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Marfan syndrome. The record also includes variant effect predictions, population frequency data, and published literature.
N98S (p.Asn98Ser) variant details
- p.Asn98Ser
- rs2505775716
- ClinGen CA392447012
- ClinVar RCV004010183
- Uncertain significance
- Marfan syndrome
- Missense
- REVEL 0.47
- CADD 25.60
- PolyPhen-2 0.96
- SIFT 0.02
- ClinVar: Uncertain significance (Marfan syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Cited in: Recommendations for physical activity and recreational sports participation for young patients with genetic… (PMID 15184297)
- Cited in: Guidelines for the diagnosis and management of Marfan syndrome. (PMID 17188935)