NM_000059.4(BRCA2):c.7868A>T (p.His2623Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001183338.3
Allele description [Variation Report for NM_000059.4(BRCA2):c.7868A>T (p.His2623Leu)]
NM_000059.4(BRCA2):c.7868A>T (p.His2623Leu)
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 MRLC2 mRNA for myosin regulatory light chain, complete cds
Homo sapiens MRLC2 mRNA for myosin regulatory light chain, complete cdsgi|20135921|dbj|D82058.1|Nucleotide
-
1567525[uid] (1)
Taxonomy
-
14q240 - Chromosomal Variation in Man
14q240 - Chromosomal Variation in Man
-
AP-1 complex subunit gamma-like 2 isoform 2 [Homo sapiens]
AP-1 complex subunit gamma-like 2 isoform 2 [Homo sapiens]gi|541862241|ref|NP_001269403.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024