NM_000251.3(MSH2):c.1821C>G (p.Ser607Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Dec 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003182924.3
Allele description [Variation Report for NM_000251.3(MSH2):c.1821C>G (p.Ser607Arg)]
NM_000251.3(MSH2):c.1821C>G (p.Ser607Arg)
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
-
holin [Bacillus phage PfEFR-5]
holin [Bacillus phage PfEFR-5]gi|1070101311|ref|YP_009285267.1|Protein
-
LOC103489938 [Cucumis melo]
LOC103489938 [Cucumis melo]Gene ID:103489938Gene
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Last Updated: May 1, 2024