Product Details

SNP ID

rs8004314

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:56122509 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGAAGCATGTGGCTCTCTTGCTGAC[C/T]AATGGCCCATGGTGGTTTTTGGAAA

Phenotype

MIM: 614798

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PELI2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115621852] 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

PELI2

Gene Name

pellino E3 ubiquitin protein ligase family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021255.2		Intron			NP_067078.1
XM_005267890.4		Intron			XP_005267947.1
XM_006720211.3		Intron			XP_006720274.1
XM_011536990.2		Intron			XP_011535292.1
XM_011536992.2		Intron			XP_011535294.1
XM_017021478.1		Intron			XP_016876967.1
XM_017021479.1		Intron			XP_016876968.1

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