Product Details

SNP ID
rs13085147
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:111732536 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAGGCCAGAGAGAGCAGGAAAGGA[A/C]ATGGAAAGGAACCTCACCTTCATGC
Phenotype
MIM: 610298 MIM: 617015
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
PHLDB2 PubMed Links
Additional Information
For this assay, SNP(s) [rs75191116] 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
PHLDB2
Gene Name
pleckstrin homology like domain family B member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001134437.1 57 UTR 5 NP_001127909.1
NM_001134438.1 57 Intron NP_001127910.1
NM_001134439.1 57 Intron NP_001127911.1
NM_145753.2 57 Intron NP_665696.1
Gene
PLCXD2
Gene Name
phosphatidylinositol specific phospholipase C X domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001185106.1 57 Intron NP_001172035.1
NM_153268.3 57 Intron NP_695000.1

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