NM_002878.4(RAD51D):c.379G>A (p.Gly127Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002365734.2
Allele description [Variation Report for NM_002878.4(RAD51D):c.379G>A (p.Gly127Ser)]
NM_002878.4(RAD51D):c.379G>A (p.Gly127Ser)
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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sediment metagenome
sediment metagenomeEstuary Sediments MetagenomeBioProject
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Protein Links for BioProject (Select 338693) (72899)
Protein
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LAMP1 lysosomal associated membrane protein 1 [Homo sapiens]
LAMP1 lysosomal associated membrane protein 1 [Homo sapiens]Gene ID:3916Gene
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Gene Links for GEO Profiles (Select 119266802) (1)
Gene
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Pirin depletion effect on myelomonocytic cell line
Pirin depletion effect on myelomonocytic cell lineAccession: GDS5254GEO DataSets
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024