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;
Origin ID : C126837;
UMLS CUI : C4289705;
Semantic type(s)
- concept_is_in_subset
- molecular_abnormality_involves_gene
