Product Details

SNP ID

rs4753827

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:108016603 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AGTGTCCTGGTGAACCCAGTTGTCA[G/T]TAAGAGCCATTTGCCTCCTGCCTTG

Phenotype

MIM: 601741

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CUL5 PubMed Links

Additional Information

For this assay, SNP(s) [rs74735899] 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

CUL5

Gene Name

cullin 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003478.3		Intron			NP_003469.2
XM_005271682.2		Intron			XP_005271739.1
XM_011543013.1		Intron			XP_011541315.1
XM_017018363.1		Intron			XP_016873852.1
XM_017018364.1		Intron			XP_016873853.1
XM_017018365.1		Intron			XP_016873854.1

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