Product Details

SNP ID

rs7027743

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:113153344 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGACCGCCTAGATTTCCATTTTGA[A/G]GCTCTCATATAATTTACTTGACCAG

Phenotype

MIM: 603088

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC31A2 PubMed Links

Additional Information

For this assay, SNP(s) [rs112831964] 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

SLC31A2

Gene Name

solute carrier family 31 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001860.2	1799	Intron			NP_001851.1
XM_011518216.1	1799	Intron			XP_011516518.1
XM_017014267.1	1799	UTR 5			XP_016869756.1

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