Product Details
- SNP ID
-
hCV31673595
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:31041181 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGTTTTAAGATCTGCCAGGAGACAT[A/T]CCCACGGGAGCTAATGGTATAGTTC
- Phenotype
-
MIM: 604611
- Polymorphism
- A/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
PURG
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs78706242] 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
- 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
There are no transcripts associated with this gene.
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