NM_000251.3(MSH2):c.2271C>T (p.Tyr757=) AND not specified
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Jul 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001358733.6
Allele description [Variation Report for NM_000251.3(MSH2):c.2271C>T (p.Tyr757=)]
NM_000251.3(MSH2):c.2271C>T (p.Tyr757=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024