NM_000059.4(BRCA2):c.7877G>A (p.Trp2626Ter) AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Jul 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000195555.17
Allele description [Variation Report for NM_000059.4(BRCA2):c.7877G>A (p.Trp2626Ter)]
NM_000059.4(BRCA2):c.7877G>A (p.Trp2626Ter)
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
-
LOC125146437 [Homo sapiens]
LOC125146437 [Homo sapiens]Gene ID:125146437Gene
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See more...Assertion and evidence details
Last Updated: Jun 23, 2024