NM_000465.4(BARD1):c.1166G>C (p.Ser389Thr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Sep 9, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000567741.7
Allele description [Variation Report for NM_000465.4(BARD1):c.1166G>C (p.Ser389Thr)]
NM_000465.4(BARD1):c.1166G>C (p.Ser389Thr)
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
-
Homo sapiens small nuclear ribonucleoprotein U5 subunit 40 (SNRNP40), mRNA
Homo sapiens small nuclear ribonucleoprotein U5 subunit 40 (SNRNP40), mRNAgi|1519473730|ref|NM_004814.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024