NM_000179.3(MSH6):c.800C>T (p.Pro267Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 5, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002419206.2
Allele description [Variation Report for NM_000179.3(MSH6):c.800C>T (p.Pro267Leu)]
NM_000179.3(MSH6):c.800C>T (p.Pro267Leu)
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
-
Homo sapiens DEAD (Asp-Glu-Ala-As) box polypeptide 19 (DDX19), mRNA
Homo sapiens DEAD (Asp-Glu-Ala-As) box polypeptide 19 (DDX19), mRNAgi|13787207|ref|NM_007242.2|Nucleotide
-
Concise Conserved Domain Links for Protein (Select 1034639365) (2)
Conserved Domains
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Last Updated: May 1, 2024