NM_000179.3(MSH6):c.3486T>G (p.Ala1162=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 12, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002454355.2
Allele description [Variation Report for NM_000179.3(MSH6):c.3486T>G (p.Ala1162=)]
NM_000179.3(MSH6):c.3486T>G (p.Ala1162=)
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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Homo sapiens adaptor-related protein complex 4, epsilon 1 subunit, mRNA (cDNA cl...
Homo sapiens adaptor-related protein complex 4, epsilon 1 subunit, mRNA (cDNA clone MGC:163338 IMAGE:40146497), complete cdsgi|120660383|gb|BC130466.1|Nucleotide
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Sample 30_LC28
Sample 30_LC28GEO DataSets
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024