NM_000179.3(MSH6):c.483G>A (p.Lys161=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000165187.5
Allele description [Variation Report for NM_000179.3(MSH6):c.483G>A (p.Lys161=)]
NM_000179.3(MSH6):c.483G>A (p.Lys161=)
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
-
12119407[uid] (0)
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Last Updated: Sep 29, 2024