Product Details

SNP ID
rs11936560
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:20702915 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGATGAGATAAATGAGATCAATGTA[C/T]TAAATCAAGGAAATTGAAATTATTC
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PACRGL PubMed Links

Gene Details

Gene
PACRGL
Gene Name
PARK2 coregulated like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130727.1 Intron NP_001124199.1
NM_001258345.1 Intron NP_001245274.1
NM_001258346.1 Intron NP_001245275.1
NM_001317849.1 Intron NP_001304778.1
NM_145048.3 Intron NP_659485.1
XM_011513780.1 Intron XP_011512082.1
XM_011513781.1 Intron XP_011512083.1
XM_011513784.1 Intron XP_011512086.1
XM_011513785.1 Intron XP_011512087.1
XM_011513786.2 Intron XP_011512088.1
XM_011513787.1 Intron XP_011512089.1
XM_011513788.1 Intron XP_011512090.1
XM_011513791.1 Intron XP_011512093.1
XM_011513792.1 Intron XP_011512094.1
XM_011513794.1 Intron XP_011512096.1
XM_011513795.1 Intron XP_011512097.1
XM_011513796.1 Intron XP_011512098.1
XM_011513797.2 Intron XP_011512099.1
XM_011513798.2 Intron XP_011512100.1
XM_011513804.1 Intron XP_011512106.1
XM_011513805.2 Intron XP_011512107.1
XM_017007747.1 Intron XP_016863236.1
XM_017007748.1 Intron XP_016863237.1
XM_017007749.1 Intron XP_016863238.1
XM_017007750.1 Intron XP_016863239.1
XM_017007751.1 Intron XP_016863240.1
XM_017007752.1 Intron XP_016863241.1
XM_017007753.1 Intron XP_016863242.1
XM_017007754.1 Intron XP_016863243.1
XM_017007755.1 Intron XP_016863244.1
XM_017007756.1 Intron XP_016863245.1
XM_017007757.1 Intron XP_016863246.1
XM_017007758.1 Intron XP_016863247.1
XM_017007759.1 Intron XP_016863248.1

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