NM_000136.3(FANCC):c.396T>C (p.Ala132=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002321128.2
Allele description [Variation Report for NM_000136.3(FANCC):c.396T>C (p.Ala132=)]
NM_000136.3(FANCC):c.396T>C (p.Ala132=)
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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Taxonomy Links for GEO Profiles (Select 103987449) (1)
Taxonomy
-
Protein Links for Nucleotide (Select 1727668143) (183)
Protein
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PMC Links for BioProject (Select 766482) (1)
PMC
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PREDICTED: Rattus norvegicus bridging integrator 1 (Bin1), transcript variant X1...
PREDICTED: Rattus norvegicus bridging integrator 1 (Bin1), transcript variant X17, mRNAgi|2678909659|ref|XM_008772014.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024