Product Details

SNP ID

rs151370

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:102253334 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCATCACGTCTCAATGGTCATAACT[A/G]TGTCATATGCCAACCTCTAACCAAT

Phenotype

MIM: 608732

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC39A8 PubMed Links

Additional Information

For this assay, SNP(s) [rs116469245] are located under a probe 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

SLC39A8

Gene Name

solute carrier family 39 member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135146.1	1787	Intron			NP_001128618.1
NM_001135147.1	1787	UTR 3			NP_001128619.1
NM_001135148.1	1787	Intron			NP_001128620.1
NM_022154.5	1787	Intron			NP_071437.3
XM_005263177.1	1787	Intron			XP_005263234.1
XM_011532181.2	1787	Intron			XP_011530483.1
XM_011532182.1	1787	Intron			XP_011530484.1
XM_017008540.1	1787	Intron			XP_016864029.1
XM_017008541.1	1787	Intron			XP_016864030.1
XM_017008542.1	1787	Intron			XP_016864031.1

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