Product Details

SNP ID
rs28749263
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:81098317 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCTATTGTGGGACCTTGTGATCG[C/T]GTGAGTTAATAAACTCCCTTTTATA
Phenotype
MIM: 601591
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRKG2 PubMed Links
Additional Information
For this assay, SNP(s) [rs113699088,rs570755798] 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
PRKG2
Gene Name
protein kinase, cGMP-dependent, type II
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282480.1 Intron NP_001269409.1
NM_001282481.1 Intron NP_001269410.1
NM_001282482.1 Intron NP_001269411.1
NM_001282483.1 Intron NP_001269412.1
NM_001282485.1 Intron NP_001269414.1
NM_006259.2 Intron NP_006250.1
XM_005263126.3 Intron XP_005263183.1
XM_017008413.1 Intron XP_016863902.1
XM_017008414.1 Intron XP_016863903.1
XM_017008415.1 Intron XP_016863904.1
XM_017008416.1 Intron XP_016863905.1
XM_017008417.1 Intron XP_016863906.1
XM_017008418.1 Intron XP_016863907.1

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