NM_000465.4(BARD1):c.1881A>C (p.Gly627=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 2, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001192174.5
Allele description [Variation Report for NM_000465.4(BARD1):c.1881A>C (p.Gly627=)]
NM_000465.4(BARD1):c.1881A>C (p.Gly627=)
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
-
MAG: Comamonadaceae bacterium CG_4_9_14_3_um_filter_60_33 CG_4_9_14_3_um_filter_...
MAG: Comamonadaceae bacterium CG_4_9_14_3_um_filter_60_33 CG_4_9_14_3_um_filter_150_scaffold_1169_c, whole genome shotgun sequencegi|1278639112|gb|PFUD01000010.1||gn :PFUD01|CG_4_9_14_3_um_filter_150_scaffold_1169_cNucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024