NM_058216.3(RAD51C):c.395C>T (p.Thr132Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 22, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000213453.3
Allele description [Variation Report for NM_058216.3(RAD51C):c.395C>T (p.Thr132Ile)]
NM_058216.3(RAD51C):c.395C>T (p.Thr132Ile)
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
-
MHC class II transactivator isoform 2 [Homo sapiens]
MHC class II transactivator isoform 2 [Homo sapiens]gi|156938336|ref|NP_000237.2|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024