Product Details

SNP ID
rs200800209
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:9782864 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGCTGCCGGAGCAGCGCAGCCTGC[A/G]CGCCCGACACCAGCCTGCGCGCTTC
Phenotype
MIM: 126453 MIM: 606142
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DRD5 PubMed Links

Gene Details

Gene
DRD5
Gene Name
dopamine receptor D5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000798.4 1231 Missense Mutation ACG,GCG T279A NP_000789.1
Gene
SLC2A9
Gene Name
solute carrier family 2 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001290.1 1231 Intron NP_001001290.1
NM_020041.2 1231 Intron NP_064425.2
XM_006713968.3 1231 Intron XP_006714031.1
XM_006713969.2 1231 Intron XP_006714032.1
XM_011513856.2 1231 Intron XP_011512158.1
XM_011513857.1 1231 Intron XP_011512159.1
XM_011513858.1 1231 Intron XP_011512160.1
XM_011513859.2 1231 Intron XP_011512161.1
XM_011513860.2 1231 Intron XP_011512162.1
XM_011513861.2 1231 Intron XP_011512163.1
XM_011513862.2 1231 Intron XP_011512164.1
XM_011513863.2 1231 Intron XP_011512165.1
XM_011513864.2 1231 Intron XP_011512166.1
XM_011513865.2 1231 Intron XP_011512167.1
XM_011513866.2 1231 Intron XP_011512168.1
XM_011513867.2 1231 Intron XP_011512169.1
XM_011513868.2 1231 Intron XP_011512170.1
XM_017008457.1 1231 Intron XP_016863946.1
XM_017008458.1 1231 Intron XP_016863947.1
XM_017008459.1 1231 Intron XP_016863948.1
XM_017008460.1 1231 Intron XP_016863949.1

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