NM_000251.3(MSH2):c.198C>T (p.Tyr66=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (3 submissions)
- Last evaluated:
- Jun 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000160652.11
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:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
olfactory receptor 2A1/2A42 [Homo sapiens]
olfactory receptor 2A1/2A42 [Homo sapiens]gi|52627213|ref|NP_001005287.1|Protein
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Last Updated: Oct 13, 2024