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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