Product Details

SNP ID

rs11594574

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:17952237 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TACATGCCTTAAGCCATCAACAGAA[A/G]GATAATTTTTTTTTCCAGGAAGTTG

Phenotype

MIM: 608734

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC39A12 PubMed Links

Additional Information

For this assay, SNP(s) [rs74642760] 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

SLC39A12

Gene Name

solute carrier family 39 member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145195.1		Intron			NP_001138667.1
NM_001282733.1		Intron			NP_001269662.1
NM_001282734.1		Intron			NP_001269663.1
NM_152725.3		Intron			NP_689938.2

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