NM_000179.3(MSH6):c.177C>T (p.Pro59=) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001425211.13
Allele description [Variation Report for NM_000179.3(MSH6):c.177C>T (p.Pro59=)]
NM_000179.3(MSH6):c.177C>T (p.Pro59=)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
Assertion and evidence details
Last Updated: Aug 4, 2024