NM_000179.3(MSH6):c.3594C>A (p.Ala1198=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003477078.1
Allele description [Variation Report for NM_000179.3(MSH6):c.3594C>A (p.Ala1198=)]
NM_000179.3(MSH6):c.3594C>A (p.Ala1198=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jan 6, 2024