NRAS NM_002524.4:c.37G C

Preferred Label : NRAS NM_002524.4:c.37G C;

NCIt synonyms : NM_002524.4:c.37G C; Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.37G C; N-ras c.37G C; NRAS c.37G C; NRAS1 c.37G C;

NCIt related terms : NRAS G13R (c.37G C) mutation;

NCIt definition : A nucleotide substitution at position 37 of the coding sequence of the NRAS gene where guanine has been mutated to cytosine.;

NCI Metathesaurus CUI : CL556284;

SNP ID : rs121434595;

Details

Origin ID

C155674;

UMLS CUI

C4744318;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Melanoma Baseline Form [NCIt concept]
- CPTAC Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- NRAS NP_002515.1:p.G13R [NCIt concept]
- NRAS Protein Variant [NCIt concept]
molecular_abnormality_involves_gene
- NRAS Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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