NM_000179.3(MSH6):c.3500T>A (p.Leu1167His) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 27, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001020468.3
Allele description [Variation Report for NM_000179.3(MSH6):c.3500T>A (p.Leu1167His)]
NM_000179.3(MSH6):c.3500T>A (p.Leu1167His)
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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Rattus norvegicus radial spoke head 14 homolog (Rsph14), transcript variant 1, mRNAgi|402693440|ref|NM_001127557.2|Nucleotide
-
T-cell leukemia homeobox protein 3 [Homo sapiens]
T-cell leukemia homeobox protein 3 [Homo sapiens]gi|50355978|ref|NP_066305.2|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024