BRAF NM_004333.4:c.1796_1797insTAC

Preferred Label : BRAF NM_004333.4:c.1796_1797insTAC;

NCIt synonyms : BRAF c.1796_1797insTAC; v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1796_1797insTAC; BRAF c.1798insTAC; NM_004333.4:c.1796_1797insTAC; B-RAF c.1796_1797insTAC; NM_004333.6:c.1794_1796dup;

NCIt definition : A genetic variation where the trinucleotide, thymine-adenine-cytosine, has been inserted between the nucleotides at positions 1796 and 1797 of the coding sequence of the BRAF gene.;

Details

Origin ID

C118896;

UMLS CUI

C3899968;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- BRAF NP_004324.2:p.T599_V600insT [NCIt concept]
- BRAF Protein Variant [NCIt concept]
molecular_abnormality_involves_gene
- BRAF Gene [NCIt concept]

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