Product Details

SNP ID
rs17065316
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:58871001 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTCAAGATTGGTAGTAATGAACATA[A/C]AACAGAGAGGATAGAAGAAAGGTGT
Phenotype
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
ZNF532 PubMed Links
Additional Information
For this assay, SNP(s) [rs75955231] 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
ZNF532
Gene Name
zinc finger protein 532
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318726.1 Intron NP_001305655.1
NM_001318727.1 Intron NP_001305656.1
NM_001318728.1 Intron NP_001305657.1
NM_018181.5 Intron NP_060651.2
XM_011526054.2 Intron XP_011524356.1
XM_011526067.2 Intron XP_011524369.1
XM_017025809.1 Intron XP_016881298.1
XM_017025810.1 Intron XP_016881299.1
XM_017025811.1 Intron XP_016881300.1
XM_017025812.1 Intron XP_016881301.1
XM_017025813.1 Intron XP_016881302.1
XM_017025814.1 Intron XP_016881303.1
XM_017025815.1 Intron XP_016881304.1
XM_017025816.1 Intron XP_016881305.1
XM_017025817.1 Intron XP_016881306.1
XM_017025818.1 Intron XP_016881307.1
XM_017025819.1 Intron XP_016881308.1
XM_017025820.1 Intron XP_016881309.1
XM_017025821.1 Intron XP_016881310.1
XM_017025822.1 Intron XP_016881311.1
XM_017025823.1 Intron XP_016881312.1
XM_017025824.1 Intron XP_016881313.1
XM_017025825.1 Intron XP_016881314.1
XM_017025826.1 Intron XP_016881315.1
XM_017025827.1 Intron XP_016881316.1
XM_017025828.1 Intron XP_016881317.1
XM_017025829.1 Intron XP_016881318.1
XM_017025830.1 Intron XP_016881319.1
XM_017025831.1 Intron XP_016881320.1

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