Product Details

SNP ID

rs6122831

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:49817727 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTAGAAACTTATAAACCGATACTGA[A/G]AAAGTACACAGACCAGAAGTATACA

Phenotype

MIM: 612730

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC9A8 PubMed Links

Additional Information

For this assay, SNP(s) [rs75873138] 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

SLC9A8

Gene Name

solute carrier family 9 member A8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001260491.1		Intron			NP_001247420.1
NM_015266.2		Intron			NP_056081.1
XM_006723756.1		Intron			XP_006723819.1
XM_011528736.1		Intron			XP_011527038.1
XM_011528737.1		Intron			XP_011527039.1
XM_011528738.1		Intron			XP_011527040.1
XM_011528739.1		Intron			XP_011527041.1
XM_011528740.1		Intron			XP_011527042.1
XM_011528741.1		Intron			XP_011527043.1
XM_011528742.1		Intron			XP_011527044.1
XM_011528743.2		Intron			XP_011527045.1
XM_011528744.2		Intron			XP_011527046.1
XM_011528745.1		Intron			XP_011527047.1
XM_017027754.1		Intron			XP_016883243.1
XM_017027755.1		Intron			XP_016883244.1
XM_017027756.1		Intron			XP_016883245.1

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