NM_000179.3(MSH6):c.2300C>G (p.Thr767Ser) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004002290.2
Allele description [Variation Report for NM_000179.3(MSH6):c.2300C>G (p.Thr767Ser)]
NM_000179.3(MSH6):c.2300C>G (p.Thr767Ser)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
Assertion and evidence details
Last Updated: Oct 26, 2024