NM_000251.3(MSH2):c.2376T>A (p.Asn792Lys) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004003745.2
Allele description [Variation Report for NM_000251.3(MSH2):c.2376T>A (p.Asn792Lys)]
NM_000251.3(MSH2):c.2376T>A (p.Asn792Lys)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
Assertion and evidence details
Last Updated: Sep 29, 2024