Product Details

SNP ID
rs2219790
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:21265191 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTAATGAATTCATGTGTTTTTCC[A/G]TAAGTTGTTTTCACCTGCTACCATT
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 6621 UTR 3 NP_066580.1
NM_134431.3 6621 UTR 3 NP_602307.1
XM_005253474.3 6621 UTR 3 XP_005253531.1
XM_005253477.3 6621 Intron XP_005253534.1
XM_011520818.1 6621 UTR 3 XP_011519120.1
XM_011520819.1 6621 UTR 3 XP_011519121.1
XM_011520820.2 6621 Intron XP_011519122.1
XM_011520821.2 6621 Intron XP_011519123.1
XM_017019849.1 6621 Intron XP_016875338.1
XM_017019850.1 6621 Intron XP_016875339.1

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