NM_144997.7(FLCN):c.161T>C (p.Met54Thr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002404768.2
Allele description [Variation Report for NM_144997.7(FLCN):c.161T>C (p.Met54Thr)]
NM_144997.7(FLCN):c.161T>C (p.Met54Thr)
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: Glycine max uncharacterized LOC100819106 (LOC100819106), mRNA
PREDICTED: Glycine max uncharacterized LOC100819106 (LOC100819106), mRNAgi|2027527704|ref|XM_014772083.3|Nucleotide
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Last Updated: Sep 29, 2024