NM_003977.4(AIP):c.784GAC[1] (p.Asp263del) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002464041.1
Allele description [Variation Report for NM_003977.4(AIP):c.784GAC[1] (p.Asp263del)]
NM_003977.4(AIP):c.784GAC[1] (p.Asp263del)
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
-
Rattus norvegicus MLLT1, super elongation complex subunit (Mllt1), mRNA
Rattus norvegicus MLLT1, super elongation complex subunit (Mllt1), mRNAgi|1937877801|ref|NM_001106876.2|Nucleotide
-
SRX4823396 (1)
SRA
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Last Updated: Sep 29, 2024