Product Details

SNP ID

rs4934529

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:35013448 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGGGAATTTTCGGAGAGAATGCA[A/T]AGTTACACATTCTAATGGTTTAAGA

Phenotype

MIM: 603135

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

CUL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs112186161] 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

CUL2

Gene Name

cullin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198777.1		Intron			NP_001185706.1
NM_001198778.1		Intron			NP_001185707.1
NM_001198779.1		Intron			NP_001185708.1
NM_001324375.1		Intron			NP_001311304.1
NM_001324376.1		Intron			NP_001311305.1
NM_003591.3		Intron			NP_003582.2
XM_011519743.1		Intron			XP_011518045.1
XM_011519744.1		Intron			XP_011518046.1
XM_011519745.1		Intron			XP_011518047.1
XM_011519747.1		Intron			XP_011518049.1

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