Product Details

SNP ID

rs10147032

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:33926682 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCATGGGCAAAATTTAATGTTACA[A/T]TTGACTGGTTAACATTAATAGGAAA

Phenotype

MIM: 606426

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

EGLN3 PubMed Links

Additional Information

For this assay, SNP(s) [rs79680493] 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

EGLN3

Gene Name

egl-9 family hypoxia inducible factor 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308103.1		Intron			NP_001295032.1
NM_022073.3		Intron			NP_071356.1

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