NM_000251.3(MSH2):c.198C>T (p.Tyr66=) AND MSH2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004544470.2
Allele description [Variation Report for NM_000251.3(MSH2):c.198C>T (p.Tyr66=)]
NM_000251.3(MSH2):c.198C>T (p.Tyr66=)
Condition(s)
- Name:
- MSH2-related disorder
- Identifiers:
-
Synthetic construct Homo sapiens clone IMAGE:100015973, MGC:184108 secretin (SCT...
Synthetic construct Homo sapiens clone IMAGE:100015973, MGC:184108 secretin (SCT) mRNA, encodes complete proteingi|157169571|gb|BC152725.1|Nucleotide
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Last Updated: Oct 13, 2024