NM_000179.3(MSH6):c.168G>T (p.Gly56=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003159723.2
Allele description [Variation Report for NM_000179.3(MSH6):c.168G>T (p.Gly56=)]
NM_000179.3(MSH6):c.168G>T (p.Gly56=)
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
-
integrin beta-1-like isoform X1 [Takifugu flavidus]
integrin beta-1-like isoform X1 [Takifugu flavidus]gi|2515658752|ref|XP_056869409.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024