Product Details

SNP ID

rs2074574

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:985997 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGGTAAGAGGAGCAAAGCGTGAG[C/G]GTTTCCCACAGGACATCTCAGCCCA

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

WDR18 PubMed Links

Additional Information

For this assay, SNP(s) [rs80201716] are located under a probe 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

WDR18

Gene Name

WD repeat domain 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024100.3		Intron			NP_077005.2
XM_017027027.1		Intron			XP_016882516.1

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