NM_000251.3(MSH2):c.2378A>C (p.Gln793Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 12, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001284508.1
Allele description [Variation Report for NM_000251.3(MSH2):c.2378A>C (p.Gln793Pro)]
NM_000251.3(MSH2):c.2378A>C (p.Gln793Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024