NM_000136.3(FANCC):c.67G>T (p.Asp23Tyr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 7, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002369487.2
Allele description [Variation Report for NM_000136.3(FANCC):c.67G>T (p.Asp23Tyr)]
NM_000136.3(FANCC):c.67G>T (p.Asp23Tyr)
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
-
peptidase inhibitor R3HDML precursor [Homo sapiens]
peptidase inhibitor R3HDML precursor [Homo sapiens]gi|30425410|ref|NP_848586.1|Protein
-
Mctp2 multiple C2 and transmembrane domain containing 2 [Rattus norvegicus]
Mctp2 multiple C2 and transmembrane domain containing 2 [Rattus norvegicus]Gene ID:308742Gene
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Last Updated: May 1, 2024