NM_000251.3(MSH2):c.1862G>A (p.Arg621Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 17, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001764525.2
Allele description [Variation Report for NM_000251.3(MSH2):c.1862G>A (p.Arg621Gln)]
NM_000251.3(MSH2):c.1862G>A (p.Arg621Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024