NM_003977.4(AIP):c.874C>G (p.Leu292Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002445231.2
Allele description [Variation Report for NM_003977.4(AIP):c.874C>G (p.Leu292Val)]
NM_003977.4(AIP):c.874C>G (p.Leu292Val)
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
-
Mus musculus 11 days embryo whole body cDNA, RIKEN full-length enriched library,...
Mus musculus 11 days embryo whole body cDNA, RIKEN full-length enriched library, clone:2700098C24 product:nestin, full insert sequencegi|12849488|dbj|AK012622.1|Nucleotide
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Last Updated: Sep 29, 2024