NM_000251.3(MSH2):c.891C>G (p.Ser297Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000563882.9
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 cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
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