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SNP ID:
rs4149056
Gene
SLCO1B1
Gene Name
Set Membership:
> HapMap > DME > Validated > Inventoried
Chromosome Location:
Chr.12: 21178615 - 21178615 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

TCTGGGTCATACATGTGGATATATG[C/T]GTTCATGGGTAATATGCTTCGTGGA

Assay ID C__30633906_10
Size 150 rxns
Availability Inventoried
Catalog # 4362691
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 604843

Literature Links:

 SLCO1B1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.09)
(0.91)
Caucasian
C (0.13)
(0.87)
CEPH (CEU)
C (0.15)
(0.85)
EAS
C (0.12)
(0.88)
African American
C (0.02)
(0.98)
YRI (Yoruba)
C (0.01)
(0.99)
SAS
C (0.04)
(0.96)
Japanese
C (0.19)
(0.81)
JPT (Japanese)
C (0.11)
(0.89)
AFR
C (0.01)
(0.99)
Chinese
C (0.12)
(0.88)
CHB (Han Chinese)
C (0.16)
(0.84)
EUR
C (0.16)
(0.84)
AMR
C (0.13)
(0.87)
SLCO1B1 - solute carrier organic anion transporter family member 1B1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_006446.4 625 Missense Mutation GCG,GTG A,V 174 NP_006437.3

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