Product Details

SNP ID

rs7119852

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:13290561 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTGCCAGCATTACAAGTGTATAT[A/G]TTATTATTATTATTATTATTATTAT

Phenotype

MIM: 602550

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ARNTL PubMed Links

Additional Information

For this assay, SNP(s) [rs535338884] 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

ARNTL

Gene Name

aryl hydrocarbon receptor nuclear translocator like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001030272.2		Intron			NP_001025443.1
NM_001030273.2		Intron			NP_001025444.1
NM_001178.5		Intron			NP_001169.3
NM_001297719.1		Intron			NP_001284648.1
NM_001297722.1		Intron			NP_001284651.1
NM_001297724.1		Intron			NP_001284653.1
XM_006718233.3		Intron			XP_006718296.1
XM_006718234.1		Intron			XP_006718297.1
XM_011520105.2		Intron			XP_011518407.2
XM_011520107.2		Intron			XP_011518409.2
XM_011520108.1		Intron			XP_011518410.1
XM_011520109.1		Intron			XP_011518411.1
XM_011520110.1		Intron			XP_011518412.1
XM_011520111.1		Intron			XP_011518413.1
XM_011520112.2		Intron			XP_011518414.1
XM_011520113.1		Intron			XP_011518415.1
XM_017017738.1		Intron			XP_016873227.1
XM_017017739.1		Intron			XP_016873228.1
XM_017017740.1		Intron			XP_016873229.1
XM_017017741.1		Intron			XP_016873230.1
XM_017017742.1		Intron			XP_016873231.1
XM_017017743.1		Intron			XP_016873232.1
XM_017017744.1		Intron			XP_016873233.1
XM_017017745.1		Intron			XP_016873234.1
XM_017017746.1		Intron			XP_016873235.1
XM_017017747.1		Intron			XP_016873236.1
XM_017017748.1		Intron			XP_016873237.1

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