Product Details

SNP ID
rs13144
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:132769632 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGATCATAAGTGAACGTAGGTTAC[A/C]AAAATGGAAGTTGTAAGTATTGTTA
Phenotype
MIM: 613361 MIM: 603571
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
SLC18B1 PubMed Links
Additional Information
For this assay, SNP(s) [rs80197282] 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
SLC18B1
Gene Name
solute carrier family 18 member B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052831.2 2161 UTR 3 NP_439896.1
XM_017010236.1 2161 UTR 3 XP_016865725.1
Gene
VNN2
Gene Name
vanin 2
There are no transcripts associated with this gene.

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