Product Details

SNP ID
rs418439
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:2901372 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGCCTCTGCGATGTCCGTCCCACCC[A/T]GTCTCACCCCTGCAGTTTTCTGCTC
Phenotype
MIM: 602631 MIM: 603240
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
SLC22A18 PubMed Links
Additional Information
For this assay, SNP(s) [rs77284315] 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
SLC22A18
Gene Name
solute carrier family 22 member 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001315501.1 Intron NP_001302430.1
NM_001315502.1 Intron NP_001302431.1
NM_002555.5 Intron NP_002546.3
NM_183233.2 Intron NP_899056.2
XM_011520141.2 Intron XP_011518443.2
XM_011520142.2 Intron XP_011518444.2
Gene
SLC22A18AS
Gene Name
solute carrier family 22 member 18 antisense
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001302862.1 Intron NP_001289791.1
NM_007105.3 Intron NP_009036.2
XM_017017832.1 Intron XP_016873321.1
XM_017017833.1 Intron XP_016873322.1
XM_017017834.1 Intron XP_016873323.1
XM_017017835.1 Intron XP_016873324.1
XM_017017836.1 Intron XP_016873325.1

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