NM_000251.3(MSH2):c.891C>G (p.Ser297Arg) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000456430.10
Allele description [Variation Report for NM_000251.3(MSH2):c.891C>G (p.Ser297Arg)]
NM_000251.3(MSH2):c.891C>G (p.Ser297Arg)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens zinc finger protein 365 (ZNF365), transcript variant B, mRNA
Homo sapiens zinc finger protein 365 (ZNF365), transcript variant B, mRNAgi|1890333717|ref|NM_199450.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024