Product Details

SNP ID

rs1509229

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:182945728 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATTCTGTGGCCATCTCACAAAGGA[A/G]ATTAACAGGAAGTGTCAAATTCCAT

Phenotype

MIM: 605905

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCUN1D1 PubMed Links

Additional Information

For this assay, SNP(s) [rs118057477] 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

DCUN1D1

Gene Name

defective in cullin neddylation 1 domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308101.1		Intron			NP_001295030.1
NM_020640.3		Intron			NP_065691.2
XM_011512912.1		Intron			XP_011511214.1
XM_011512914.1		Intron			XP_011511216.1
XM_011512915.2		Intron			XP_011511217.1
XM_011512916.2		Intron			XP_011511218.1
XM_017006633.1		Intron			XP_016862122.1
XM_017006634.1		Intron			XP_016862123.1
XM_017006635.1		Intron			XP_016862124.1

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