Product Details

SNP ID
rs143932538
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:81092416 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGCAAAGGTGATGGAAGGCTCCG[C/T]GCTTTCAGTCCCTCCCAATTAAAAC
Phenotype
MIM: 601591
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRKG2 PubMed Links

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 2712 Silent Mutation GCA,GCG A301A NP_001269409.1
NM_001282481.1 2712 Silent Mutation GCA,GCG A301A NP_001269410.1
NM_001282482.1 2712 Silent Mutation GCA,GCG A272A NP_001269411.1
NM_001282483.1 2712 Silent Mutation GCA,GCG A241A NP_001269412.1
NM_001282485.1 2712 Silent Mutation GCA,GCG A692A NP_001269414.1
NM_006259.2 2712 Silent Mutation GCA,GCG A721A NP_006250.1
XM_005263126.3 2712 Silent Mutation GCA,GCG A721A XP_005263183.1
XM_017008413.1 2712 Silent Mutation GCA,GCG A721A XP_016863902.1
XM_017008414.1 2712 Silent Mutation GCA,GCG A721A XP_016863903.1
XM_017008415.1 2712 Silent Mutation GCA,GCG A721A XP_016863904.1
XM_017008416.1 2712 Silent Mutation GCA,GCG A721A XP_016863905.1
XM_017008417.1 2712 Silent Mutation GCA,GCG A692A XP_016863906.1
XM_017008418.1 2712 Intron XP_016863907.1

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