NM_000251.3(MSH2):c.841T>C (p.Ser281Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000115543.4
Allele description [Variation Report for NM_000251.3(MSH2):c.841T>C (p.Ser281Pro)]
NM_000251.3(MSH2):c.841T>C (p.Ser281Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
842597 (0)
PopSet
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Last Updated: Sep 29, 2024