NM_000251.3(MSH2):c.1954C>G (p.Pro652Ala) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000629891.6
Allele description [Variation Report for NM_000251.3(MSH2):c.1954C>G (p.Pro652Ala)]
NM_000251.3(MSH2):c.1954C>G (p.Pro652Ala)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
Assertion and evidence details
Last Updated: Feb 28, 2024