Product Details

SNP ID

rs329499

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:64096942 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGATGGAAATATGTGTATCATGTAG[G/T]TTTTTTCTCTTTAGAGATATTTAAA

Phenotype

MIM: 614797

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

PELI1 PubMed Links

Additional Information

For this assay, SNP(s) [rs74456017] 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

PELI1

Gene Name

pellino E3 ubiquitin protein ligase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020651.3		Intron			NP_065702.2
XM_005264437.3		Intron			XP_005264494.1
XM_011532994.2		Intron			XP_011531296.1
XM_011532996.2		Intron			XP_011531298.1
XM_011532997.2		Intron			XP_011531299.1
XM_017004520.1		Intron			XP_016860009.1
XM_017004521.1		Intron			XP_016860010.1

View Full Product Details