Product Details

SNP ID
rs4149008
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:21268105 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATTTGCTTTCTTTTTTCATATGAT[A/G]CATCTGATCATTTAGGAAATCATAT
Phenotype
MIM: 602883
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLCO1A2 PubMed Links

Gene Details

Gene
SLCO1A2
Gene Name
solute carrier organic anion transporter family member 1A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021094.3 3707 UTR 3 NP_066580.1
NM_134431.3 3707 UTR 3 NP_602307.1
XM_005253474.3 3707 UTR 3 XP_005253531.1
XM_005253477.3 3707 UTR 3 XP_005253534.1
XM_011520818.1 3707 UTR 3 XP_011519120.1
XM_011520819.1 3707 UTR 3 XP_011519121.1
XM_011520820.2 3707 UTR 3 XP_011519122.1
XM_011520821.2 3707 UTR 3 XP_011519123.1
XM_017019849.1 3707 Intron XP_016875338.1
XM_017019850.1 3707 Intron XP_016875339.1

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