NM_000059.4(BRCA2):c.2886T>C (p.His962=) AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000918597.9
Allele description [Variation Report for NM_000059.4(BRCA2):c.2886T>C (p.His962=)]
NM_000059.4(BRCA2):c.2886T>C (p.His962=)
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
-
ATP-dependent 6-phosphofructokinase 7-like isoform X3 [Cucurbita maxima]
ATP-dependent 6-phosphofructokinase 7-like isoform X3 [Cucurbita maxima]gi|1280981579|ref|XP_023005311.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024