NM_144997.7(FLCN):c.179C>T (p.Ala60Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002409416.2
Allele description [Variation Report for NM_144997.7(FLCN):c.179C>T (p.Ala60Val)]
NM_144997.7(FLCN):c.179C>T (p.Ala60Val)
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
-
Hepatitis B virus DNA, complete genome, strain: C0714154(WBK)F
Hepatitis B virus DNA, complete genome, strain: C0714154(WBK)Fgi|251822189|dbj|AP011098.1|Nucleotide
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Last Updated: Jun 9, 2024