NM_144997.7(FLCN):c.1149C>T (p.Leu383=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Aug 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000163531.6
Allele description [Variation Report for NM_144997.7(FLCN):c.1149C>T (p.Leu383=)]
NM_144997.7(FLCN):c.1149C>T (p.Leu383=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
Assertion and evidence details
Last Updated: Aug 4, 2024