NM_000251.3(MSH2):c.1135G>T (p.Asp379Tyr) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001237221.5
Allele description [Variation Report for NM_000251.3(MSH2):c.1135G>T (p.Asp379Tyr)]
NM_000251.3(MSH2):c.1135G>T (p.Asp379Tyr)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
MULTISPECIES: hypothetical protein [Bacillus cereus group]
MULTISPECIES: hypothetical protein [Bacillus cereus group]gi|446961849|ref|WP_001039105.1|Protein
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Last Updated: Sep 29, 2024