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BRAF NM_004333.4:c.1799T>C

MedGen UID:: 475620
•Concept ID:: C3273987
•: Cell or Molecular Dysfunction

Synonyms:

B-RAF1 c.1799T>C; BRAF c.1799T>C; NM_004333.4:c.1799T>C; v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1799T>C

Definition

A nucleotide substitution at position 1799 of the coding sequence of the BRAF gene where thymine has been mutated to cytosine. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVBRAF NM_004333.4:c.1799T>C

Molecular Sequence Variation
- Molecular Genetic Variation
  - Gene Abnormality
    - RAF Family Gene Mutation
      - BRAF Gene Mutation
        BRAF Exon 15 Mutation
        BRAF NM_004333.4:c.1799T>C

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BRAF NM_004333.4:c.1799T>C
BRAF NM_004333.4:c.1799T>C

MedGen
ERBB2 NM_004448.2:c.2325_2326ins12
ERBB2 NM_004448.2:c.2325_2326ins12

MedGen

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