BRAF NM_004333.4:c.1797_1798insACA

Preferred Label : BRAF NM_004333.4:c.1797_1798insACA;

NCIt synonyms : NM_004333.4:c.1797_1798insACA; BRAF c.1795_1797dup; BRAF c.1797_1798insACA; NM_004333.4:c.1795_1797dup; v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1797_1798insACA; B-RAF1 c.1797_1798insACA; NM_004333.4:c.1795_1797dupACA;

NCIt definition : A genetic variation where the trinucleotide, adenine-cytosine-adenine, has been inserted between the nucleotides at positions 1797 and 1798 of the coding sequence of the BRAF gene.;

Details

Origin ID

C118895;

UMLS CUI

C3899967;

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]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients