NM_000251.3(MSH2):c.2328T>C (p.Ala776=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001015203.3
Allele description [Variation Report for NM_000251.3(MSH2):c.2328T>C (p.Ala776=)]
NM_000251.3(MSH2):c.2328T>C (p.Ala776=)
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
-
Chain B, Histone H4
Chain B, Histone H4gi|2700920799|pdb|8V7L|BProtein
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See more...Assertion and evidence details
Last Updated: May 1, 2024