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t(1;3)(p36;q23-25)

MedGen UID:
881449
•Concept ID:
C4053815
•
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation of the short arm (p36) of chromosome 1 and the long arm (q23-25) of chromosome 3. It is associated with WWTR1/CAMTA1 fusions. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;3)(p36;q23-25)

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