Product Details

SNP ID

rs2014123

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:92325547 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGGCAGGGGCCCTCTGAGAGTGTC[C/T]TTTACTGGAAGAACACTTAAAAGGT

Phenotype

MIM: 609840

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC24A4 PubMed Links

Additional Information

For this assay, SNP(s) [rs117243934] 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

SLC24A4

Gene Name

solute carrier family 24 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153646.3		Intron			NP_705932.2
NM_153647.3		Intron			NP_705933.2
NM_153648.3		Intron			NP_705934.1
XM_005267342.2		Intron			XP_005267399.1
XM_011536436.2		Intron			XP_011534738.1
XM_011536437.2		Intron			XP_011534739.1
XM_011536438.2		Intron			XP_011534740.1
XM_011536439.2		Intron			XP_011534741.1
XM_011536440.2		Intron			XP_011534742.1
XM_011536441.2		Intron			XP_011534743.1
XM_011536442.2		Intron			XP_011534744.1

View Full Product Details