NM_000251.3(MSH2):c.1656C>T (p.Thr552=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 4, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000827066.1
Allele description [Variation Report for NM_000251.3(MSH2):c.1656C>T (p.Thr552=)]
NM_000251.3(MSH2):c.1656C>T (p.Thr552=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024