Product Details

SNP ID

rs8041008

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:48669897 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGATATACTGTAGTACAATATAGT[A/G]TATATATATATATATATATATATAT

Phenotype

MIM: 613529

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CEP152 PubMed Links

Additional Information

For this assay, SNP(s) [rs576225037] 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

CEP152

Gene Name

centrosomal protein 152

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001194998.1		Intron			NP_001181927.1
NM_014985.3		Intron			NP_055800.2
XM_006720437.3		Intron			XP_006720500.1
XM_011521373.2		Intron			XP_011519675.1
XM_011521374.2		Intron			XP_011519676.1
XM_011521375.2		Intron			XP_011519677.1
XM_011521378.2		Intron			XP_011519680.1
XM_011521379.2		Intron			XP_011519681.1
XM_011521381.2		Intron			XP_011519683.1
XM_017022014.1		Intron			XP_016877503.1
XM_017022015.1		Intron			XP_016877504.1
XM_017022016.1		Intron			XP_016877505.1

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