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BRAF NM_004333.4:c.1789_1790delinsTC

MedGen UID:
475616
Concept ID:
C3273983
Cell or Molecular Dysfunction
Synonyms: B-RAF1 c.1789_1790CT>TC; BRAF c.1789_1790CT>TC; BRAF c.1789_1790delCTinsTC; BRAF NM_004333.4:c.1789_1790delCTinsTC; NM_004333.4:c.1789_1790CT>TC; NM_004333.4:c.1789_1790delCTinsTC; NM_004333.4:c.1789_1790delinsTC; v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1789_1790CT>TC

Definition

A complex substitution where the nucleotide sequence at positions 1789 and 1790 of the coding sequence of the BRAF gene has changed from cytosine-thymine to thymine-cytosine. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVBRAF NM_004333.4:c.1789_1790delinsTC

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