NM_001999.4(FBN2):c.3577C>T (p.Pro1193Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001759495.2
Allele description [Variation Report for NM_001999.4(FBN2):c.3577C>T (p.Pro1193Ser)]
NM_001999.4(FBN2):c.3577C>T (p.Pro1193Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024