Product Details

SNP ID

rs7179931

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:48667717 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGGTAACTTTCTAGCAAGACAATGT[G/T]TCCAGTTTGGGAAAACTCAAGTTTA

Phenotype

MIM: 613529

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

CEP152 PubMed Links

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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