NM_000179.3(MSH6):c.1176T>C (p.Asp392=) AND Lynch syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003997442.2
Allele description [Variation Report for NM_000179.3(MSH6):c.1176T>C (p.Asp392=)]
NM_000179.3(MSH6):c.1176T>C (p.Asp392=)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
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Last Updated: Sep 29, 2024