Product Details

SNP ID: rs5332
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:175441748 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGGGATGAGCATGTGTGGCAGGATT[T/C]ATCTGCGAGTTCAGGTTGGGTGCTG
Phenotype: MIM: 126449
Polymorphism: T/C, Transition substitution
Allele Nomenclature
Literature Links: DRD1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000794.3	2297	UTR 3			NP_000785.1