Product Details
- SNP ID
-
rs1564363
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:21139930 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GAAGTGCTCTCCGGTGCACAAGAGT[G/A]TCTGAGGGAAAAGATACATATGCTG
- Phenotype
-
MIM: 604843
- Polymorphism
- G/A, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SLCO1B1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs149283616] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- SLCO1B1
- Gene Name
- solute carrier organic anion transporter family member 1B1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_006446.4 |
|
Intron |
|
|
NP_006437.3 |
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