NM_000465.4(BARD1):c.266C>G (p.Pro89Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000570063.5
Allele description [Variation Report for NM_000465.4(BARD1):c.266C>G (p.Pro89Arg)]
NM_000465.4(BARD1):c.266C>G (p.Pro89Arg)
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
-
protein Wnt-5a isoform 1 precursor [Mus musculus]
protein Wnt-5a isoform 1 precursor [Mus musculus]gi|46909567|ref|NP_033550.2|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024