NM_001999.4(FBN2):c.4983C>T (p.Cys1661=) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 11, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000125057.20
Allele description [Variation Report for NM_001999.4(FBN2):c.4983C>T (p.Cys1661=)]
NM_001999.4(FBN2):c.4983C>T (p.Cys1661=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024