NM_000059.4(BRCA2):c.5221A>G (p.Ser1741Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (3 submissions)
- Last evaluated:
- Jan 9, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000776931.8
Allele description [Variation Report for NM_000059.4(BRCA2):c.5221A>G (p.Ser1741Gly)]
NM_000059.4(BRCA2):c.5221A>G (p.Ser1741Gly)
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
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Homologene neighbors for GEO Profiles (Select 67861999) (0)
GEO Profiles
-
HFM1 helicase for meiosis 1 [Homo sapiens]
HFM1 helicase for meiosis 1 [Homo sapiens]Gene ID:164045Gene
-
Gene Links for GEO Profiles (Select 67893622) (1)
Gene
-
Caseous tuberculosis granulomas comparison with normal lung parenchyma
Caseous tuberculosis granulomas comparison with normal lung parenchymaAccession: GDS4256GEO DataSets
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Related DataSets for GEO Profiles (Select 91670417) (1)
GEO DataSets
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024