NM_000251.3(MSH2):c.207G>C (p.Pro69=) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002067308.6
Allele description [Variation Report for NM_000251.3(MSH2):c.207G>C (p.Pro69=)]
NM_000251.3(MSH2):c.207G>C (p.Pro69=)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
SGCG [Opisthocomus hoazin]
SGCG [Opisthocomus hoazin]Gene ID:104337299Gene
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Last Updated: Sep 29, 2024