NM_000251.3(MSH2):c.1864C>G (p.Pro622Ala) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Oct 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001311925.20
Allele description [Variation Report for NM_000251.3(MSH2):c.1864C>G (p.Pro622Ala)]
NM_000251.3(MSH2):c.1864C>G (p.Pro622Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024