NM_000059.4(BRCA2):c.8663G>T (p.Arg2888Leu) AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001302575.4
Allele description [Variation Report for NM_000059.4(BRCA2):c.8663G>T (p.Arg2888Leu)]
NM_000059.4(BRCA2):c.8663G>T (p.Arg2888Leu)
Condition(s)
- Name:
- Hereditary breast ovarian cancer syndrome
- Synonyms:
- Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145
-
LOC105375443 [Homo sapiens]
LOC105375443 [Homo sapiens]Gene ID:105375443Gene
-
FDBC8-1 DNA segment, FDBC8-1 [Mus musculus]
FDBC8-1 DNA segment, FDBC8-1 [Mus musculus]Gene ID:53099Gene
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Last Updated: Sep 1, 2024