NM_000179.3(MSH6):c.112C>G (p.Pro38Ala) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002013432.3
Allele description [Variation Report for NM_000179.3(MSH6):c.112C>G (p.Pro38Ala)]
NM_000179.3(MSH6):c.112C>G (p.Pro38Ala)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
Assertion and evidence details
Last Updated: May 7, 2024