NM_000179.3(MSH6):c.660A>C (p.Glu220Asp) AND Lynch syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 5, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000075020.13
Allele description [Variation Report for NM_000179.3(MSH6):c.660A>C (p.Glu220Asp)]
NM_000179.3(MSH6):c.660A>C (p.Glu220Asp)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
Assertion and evidence details
Last Updated: Mar 23, 2024