Product Details

SNP ID

rs12603270

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:55269782 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAATCCCTGTCTTCTGAAATATCTT[C/T]GTAAGGTAACTAGGTACTGTATATA

Phenotype

MIM: 142385

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HLF PubMed Links

Additional Information

For this assay, SNP(s) [rs137956874] 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

HLF

Gene Name

HLF, PAR bZIP transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002126.4		Intron			NP_002117.1
XM_005257269.2		Intron			XP_005257326.1
XM_011524705.1		Intron			XP_011523007.1
XM_017024556.1		Intron			XP_016880045.1

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