NM_144997.7(FLCN):c.1251C>T (p.Phe417=) AND Birt-Hogg-Dube syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000928229.7
Allele description [Variation Report for NM_144997.7(FLCN):c.1251C>T (p.Phe417=)]
NM_144997.7(FLCN):c.1251C>T (p.Phe417=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024