NM_000179.3(MSH6):c.4018_4032del (p.Ser1340_Thr1344del) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001526019.2
Allele description [Variation Report for NM_000179.3(MSH6):c.4018_4032del (p.Ser1340_Thr1344del)]
NM_000179.3(MSH6):c.4018_4032del (p.Ser1340_Thr1344del)
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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SLC30A7 solute carrier family 30 member 7 [Homo sapiens]
SLC30A7 solute carrier family 30 member 7 [Homo sapiens]Gene ID:148867Gene
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Gene Links for GEO Profiles (Select 121064357) (1)
Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024