NRAS NM_002524.4:c.182A T

Preferred Label : NRAS NM_002524.4:c.182A T;

NCIt synonyms : N-ras c.182A T; NM_002524.4:c.182A T; Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.182A T; NRAS c.182A T; NRAS1 c.182A T;

NCIt related terms : NRAS Q61L (c.182A T) mutation;

NCIt definition : A nucleotide substitution at position 182 of the coding sequence of the NRAS gene where adenine has been mutated to thymine.;

SNP ID : rs11554290;

Details

Origin ID

C98450;

UMLS CUI

C3274098;

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]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- NRAS NP_002515.1:p.Q61L [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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