NM_144997.7(FLCN):c.1075C>T (p.Pro359Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003163719.2
Allele description [Variation Report for NM_144997.7(FLCN):c.1075C>T (p.Pro359Ser)]
NM_144997.7(FLCN):c.1075C>T (p.Pro359Ser)
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
-
PREDICTED: Rattus norvegicus innate immunity activator (Inava), transcript varia...
PREDICTED: Rattus norvegicus innate immunity activator (Inava), transcript variant X1, mRNAgi|2678891367|ref|XM_006249920.5|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jun 9, 2024