NM_000251.3(MSH2):c.434T>C (p.Ile145Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003226296.1
Allele description [Variation Report for NM_000251.3(MSH2):c.434T>C (p.Ile145Thr)]
NM_000251.3(MSH2):c.434T>C (p.Ile145Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024