NM_000251.3(MSH2):c.2397T>C (p.Asn799=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001175570.1
Allele description [Variation Report for NM_000251.3(MSH2):c.2397T>C (p.Asn799=)]
NM_000251.3(MSH2):c.2397T>C (p.Asn799=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024