NM_144997.7(FLCN):c.42C>T (p.His14=) AND Birt-Hogg-Dube syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000227689.10
Allele description [Variation Report for NM_144997.7(FLCN):c.42C>T (p.His14=)]
NM_144997.7(FLCN):c.42C>T (p.His14=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024