Product Details

SNP ID
rs200440686
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:113410799 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTGGTGTAGATGATGGGGTTCAC[A/G]GCGCTGTTGACATAGCCCAGCCACG
Phenotype
MIM: 126450
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DRD2 PubMed Links

Gene Details

Gene
DRD2
Gene Name
dopamine receptor D2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000795.3 1477 Silent Mutation GCC,GCT A420A NP_000786.1
NM_016574.3 1477 Silent Mutation GCC,GCT A391A NP_057658.2
XM_017017296.1 1477 Silent Mutation GCC,GCT A420A XP_016872785.1

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