NM_000179.3(MSH6):c.116G>C (p.Gly39Ala) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000823347.9
Allele description [Variation Report for NM_000179.3(MSH6):c.116G>C (p.Gly39Ala)]
NM_000179.3(MSH6):c.116G>C (p.Gly39Ala)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
Assertion and evidence details
Last Updated: Sep 29, 2024