NM_000251.2(MSH2):c.2131C>T (p.Arg711Ter) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Feb 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000129341.3
Allele description
NM_000251.2(MSH2):c.2131C>T (p.Arg711Ter)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition
- Identifiers:
- MedGen: C0027672
Assertion and evidence details
Last Updated: Jun 15, 2017