Product Details

SNP ID
rs13269094
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:31038635 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATCATACCTAATTCCCAAATCCAA[G/T]GCCATGAAGATTTTCTGTTATGTTT
Phenotype
MIM: 604611
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
PURG PubMed Links

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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