NM_000136.3(FANCC):c.546C>T (p.Ser182=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002349772.2
Allele description [Variation Report for NM_000136.3(FANCC):c.546C>T (p.Ser182=)]
NM_000136.3(FANCC):c.546C>T (p.Ser182=)
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
-
Mus musculus alanyl-tRNA synthetase 2, mitochondrial (Aars2), transcript variant...
Mus musculus alanyl-tRNA synthetase 2, mitochondrial (Aars2), transcript variant 1, mRNA; nuclear gene for mitochondrial productgi|2777372328|ref|NM_198608.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024