NM_000179.3(MSH6):c.968C>T (p.Thr323Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Aug 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000579969.10
Allele description [Variation Report for NM_000179.3(MSH6):c.968C>T (p.Thr323Ile)]
NM_000179.3(MSH6):c.968C>T (p.Thr323Ile)
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
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Homologene neighbors for GEO Profiles (Select 57665122) (0)
GEO Profiles
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Profile neighbors for GEO Profiles (Select 132566162) (165)
GEO Profiles
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Component(Core) Links for Nucleotide (Select 255522790) (3)
Nucleotide
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Concise Conserved Domain Links for Protein (Select 1778700917) (1)
Conserved Domains
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PubChem Substance Links for Gene (Select 375295) (60)
PubChem Substance
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See more...Assertion and evidence details
Last Updated: May 7, 2024