NM_000136.3(FANCC):c.700C>G (p.Leu234Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002365813.2
Allele description [Variation Report for NM_000136.3(FANCC):c.700C>G (p.Leu234Val)]
NM_000136.3(FANCC):c.700C>G (p.Leu234Val)
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
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Pcyt2 phosphate cytidylyltransferase 2, ethanolamine [Mus musculus]
Pcyt2 phosphate cytidylyltransferase 2, ethanolamine [Mus musculus]Gene ID:68671Gene
-
Gene Links for GEO Profiles (Select 91479799) (1)
Gene
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Last Updated: May 1, 2024