Product Details

SNP ID

rs12304867

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:100474905 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTGTTTCTGGTGCTGTCTTAGAA[C/T]CACTTCAGGAGTATTGACAAGAGGG

Phenotype

MIM: 603826

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NR1H4 PubMed Links

Additional Information

For this assay, SNP(s) [rs142975098] 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

NR1H4

Gene Name

nuclear receptor subfamily 1 group H member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206977.1		Intron			NP_001193906.1
NM_001206978.1		Intron			NP_001193907.1
NM_001206979.1		Intron			NP_001193908.1
NM_001206992.1		Intron			NP_001193921.1
NM_001206993.1		Intron			NP_001193922.1
NM_005123.3		Intron			NP_005114.1
XM_006719719.2		Intron			XP_006719782.1
XM_011539040.2		Intron			XP_011537342.1
XM_011539041.2		Intron			XP_011537343.1
XM_011539042.1		Intron			XP_011537344.1

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