NM_000179.3(MSH6):c.818G>T (p.Gly273Val) AND Hereditary cancer
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003491994.1
Allele description [Variation Report for NM_000179.3(MSH6):c.818G>T (p.Gly273Val)]
NM_000179.3(MSH6):c.818G>T (p.Gly273Val)
Condition(s)
- Name:
- Hereditary cancer
- Identifiers:
- MedGen: C1333600
Assertion and evidence details
Last Updated: Sep 16, 2024