Product Details

SNP ID

rs115157134

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:84126791 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGCTGAAAATGAAGTTGGCACTT[G/T]CTTTAATGCATTAAGTTTCACTACA

Phenotype

MIM: 610201 MIM: 615410

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CEP162 PubMed Links

Additional Information

For this assay, SNP(s) [rs140862528] 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

CEP162

Gene Name

centrosomal protein 162

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286206.1		Intron			NP_001273135.1
NM_014895.3		Intron			NP_055710.2
XM_005248674.3		Intron			XP_005248731.1
XM_005248678.3		Intron			XP_005248735.1
XM_006715380.2		Intron			XP_006715443.1
XM_011535592.2		Intron			XP_011533894.1
XM_011535594.2		Intron			XP_011533896.1
XM_017010483.1		Intron			XP_016865972.1
XM_017010484.1		Intron			XP_016865973.1

Gene

MRAP2

Gene Name

melanocortin 2 receptor accessory protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138409.2		Intron			NP_612418.2
XM_011535400.2		Intron			XP_011533702.1
XM_017010219.1		Intron			XP_016865708.1
XM_017010220.1		Intron			XP_016865709.1
XM_017010221.1		Intron			XP_016865710.1

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