NM_144997.7(FLCN):c.1288G>T (p.Val430Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002383244.2
Allele description [Variation Report for NM_144997.7(FLCN):c.1288G>T (p.Val430Leu)]
NM_144997.7(FLCN):c.1288G>T (p.Val430Leu)
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
-
LOC106585549 [Salmo salar]
LOC106585549 [Salmo salar]Gene ID:106585549Gene
-
LOC120147129 [Hibiscus syriacus]
LOC120147129 [Hibiscus syriacus]Gene ID:120147129Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024