Product Details

SNP ID

rs35529280

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:31041738 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

TAGGAGGGGAGGATAGTAAATAGAT[G/T]AGGGAAAAGTTGTAGGATTGCCAGG

Phenotype

MIM: 604611

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

PURG PubMed Links

Additional Information

For this assay, SNP(s) [rs77145852] 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

PURG

Gene Name

purine rich element binding protein G

There are no transcripts associated with this gene.

Gene

WRN

Gene Name

Werner syndrome RecQ like helicase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000553.4		Intron			NP_000544.2
XM_011544639.2		Intron			XP_011542941.1
XM_011544640.1		Intron			XP_011542942.1

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