NM_000465.4(BARD1):c.1993G>A (p.Glu665Lys) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 27, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000216543.3
Allele description [Variation Report for NM_000465.4(BARD1):c.1993G>A (p.Glu665Lys)]
NM_000465.4(BARD1):c.1993G>A (p.Glu665Lys)
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
-
1q42.1 (0)
OMIM
-
Homo sapiens cDNA FLJ32323 fis, clone PROST2003674
Homo sapiens cDNA FLJ32323 fis, clone PROST2003674gi|16552406|dbj|AK056885.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024