Product Details

SNP ID

rs12418061

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63083064 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CACGGCTGACATTGATTGAGTAAGA[A/G]CCCAAGTGCTGAAAACAACATATTG

Phenotype

MIM: 611698

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC22A24 PubMed Links

Additional Information

For this assay, SNP(s) [rs115492125] 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

SLC22A24

Gene Name

solute carrier family 22 member 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136506.2		Intron			NP_001129978.2
NM_173586.2		Intron			NP_775857.2
XM_011544967.2		Intron			XP_011543269.1

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