Product Details

SNP ID

rs12003423

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.9:84274729 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACCAGAGACAGTTATTGAGTCCTAC[A/G]CTCCTACCTTTGTAAAATGTGAGTG

Phenotype

MIM: 608269

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC28A3 PubMed Links

Additional Information

For this assay, SNP(s) [rs74751620] 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

SLC28A3

Gene Name

solute carrier family 28 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199633.1	5616	Intron			NP_001186562.1
NM_022127.2	5616	Intron			NP_071410.1
XM_011518905.2	5616	UTR 3			XP_011517207.1
XM_011518906.2	5616	UTR 3			XP_011517208.1
XM_011518907.2	5616	UTR 3			XP_011517209.1
XM_011518908.2	5616	UTR 3			XP_011517210.1
XM_011518909.2	5616	Intron			XP_011517211.1
XM_011518910.2	5616	Intron			XP_011517212.1

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