Product Details

SNP ID
rs145125600
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:48472886 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAAGAAGCTTGAACTAAGCAGTAA[C/G]AGAGCCTCAGTGGGCCTAGAAGTAT
Phenotype
MIM: 606878
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
ANP32D PubMed Links
Additional Information
For this assay, SNP(s) [rs7956679] are located under a primer 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
ANP32D
Gene Name
acidic nuclear phosphoprotein 32 family member D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012404.2 Intron NP_036536.2
Gene
C12orf54
Gene Name
chromosome 12 open reading frame 54
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152319.3 Intron NP_689532.1
XM_005268636.3 Intron XP_005268693.1
XM_011537896.2 Intron XP_011536198.1
XM_017018796.1 Intron XP_016874285.1

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