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BRAF NM_004333.4:c.1799_1800delinsAT

MedGen UID:
475622
Concept ID:
C3273989
Cell or Molecular Dysfunction
Synonyms: B-RAF1 c.1799_1800TG>AT; BRAF c.1799_1800delTGinsAT; BRAF c.1799_1800TG>AT; BRAF NM_004333.4:c.1799_1800delTGinsAT; NM_004333.4:c.1799_1800delinsAT; NM_004333.4:c.1799_1800delTGinsAT; NM_004333.4:c.1799_1800TG>AT; NM_004333.6:c.1799_1800delinsAT; v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1799_1800TG>AT

Definition

A complex substitution where the nucleotide sequence at positions 1799 and 1780 of the coding sequence of the BRAF gene has changed from thymine-guanine to adenine-thymine. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVBRAF NM_004333.4:c.1799_1800delinsAT

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