NM_000179.3(MSH6):c.3886A>G (p.Lys1296Glu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001290552.1
Allele description [Variation Report for NM_000179.3(MSH6):c.3886A>G (p.Lys1296Glu)]
NM_000179.3(MSH6):c.3886A>G (p.Lys1296Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024