Product Details

SNP ID
rs149843
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:38285166 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTTTGGCTGTGGAAAATACTAAGA[A/G]CAAGTAGTAGCAGGCAGAAGTTCAC
Phenotype
MIM: 604047 MIM: 604048
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC22A13 PubMed Links
Additional Information
For this assay, SNP(s) [rs111389039] are located under a primer 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
SLC22A13
Gene Name
solute carrier family 22 member 13
There are no transcripts associated with this gene.

Gene
SLC22A14
Gene Name
solute carrier family 22 member 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320033.1 Intron NP_001306962.1
NM_004803.4 Intron NP_004794.2
XM_005265585.4 Intron XP_005265642.1
XM_006713416.3 Intron XP_006713479.2
XM_006713417.3 Intron XP_006713480.2
XM_006713418.3 Intron XP_006713481.2
XM_011534245.2 Intron XP_011532547.1
XM_011534247.2 Intron XP_011532549.1

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