DRD2 NM_000795.3:c.957C T

Preferred Label : DRD2 NM_000795.3:c.957C T;

NCIt synonyms : DRD2 c.957C T; NM_000795.3:c.957C T; DRD2 957T Indel Mutation; Dopamine Receptor D2 c.957C T; DRD2 C957T Indel Mutation;

NCIt definition : A nucleotide substitution at position 957 of the coding sequence of the DRD2 gene where cytosine has been mutated to thymine.;

NCIt note : The DRD2 c.957C T substitution mutant is a synonymous polymorphism that appears to decrease the stability of the mRNA.;

NCI Metathesaurus CUI : CL508120;

SNP ID : rs6277;

Details

Origin ID

C126837;

UMLS CUI

C4289705;

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]
molecular_abnormality_involves_gene
- DRD2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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