NM_024675.4(PALB2):c.567A>G (p.Arg189=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003584967.1
Allele description [Variation Report for NM_024675.4(PALB2):c.567A>G (p.Arg189=)]
NM_024675.4(PALB2):c.567A>G (p.Arg189=)
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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CCDC66 coiled-coil domain containing 66 [Homo sapiens]
CCDC66 coiled-coil domain containing 66 [Homo sapiens]Gene ID:285331Gene
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Gene Links for GEO Profiles (Select 39287477) (1)
Gene
-
Related DataSets for GEO Profiles (Select 39260645) (1)
GEO DataSets
-
Endometriosis
EndometriosisAccession: GDS2737GEO DataSets
-
Rheumatoid arthritis and osteoarthritis: synovial fibroblasts
Rheumatoid arthritis and osteoarthritis: synovial fibroblastsAccession: GDS2931GEO DataSets
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024