Product Details

SNP ID

rs3848599

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:33144981 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGGAAGAGGGAGGGTGAGCAGGCA[G/T]GCCATAAATAGGTATGCCTGTGACA

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

WDR88 PubMed Links

Additional Information

For this assay, SNP(s) [rs3848597] 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

WDR88

Gene Name

WD repeat domain 88

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173479.3		Intron			NP_775750.3
XM_011526449.2		Intron			XP_011524751.1
XM_011526450.2		Intron			XP_011524752.1
XM_017026282.1		Intron			XP_016881771.1
XM_017026283.1		Intron			XP_016881772.1

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