NM_000179.3(MSH6):c.178T>C (p.Leu60=) AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000212625.9
Allele description [Variation Report for NM_000179.3(MSH6):c.178T>C (p.Leu60=)]
NM_000179.3(MSH6):c.178T>C (p.Leu60=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 20, 2024