Product Details

SNP ID

rs12587742

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:72926683 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGGAGGGGCGGGGAGGAGTGAGCAC[A/G]TGGAACGCCGGCGCCACCGGGCCTA

Phenotype

MIM: 616372

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCAF4 PubMed Links

Additional Information

For this assay, SNP(s) [rs201827930] 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

DCAF4

Gene Name

DDB1 and CUL4 associated factor 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163508.1		Intron			NP_001156980.1
NM_001163509.1		Intron			NP_001156981.1
NM_015604.3		Intron			NP_056419.2
NM_181340.2		Intron			NP_851937.1
NM_181341.2		Intron			NP_851938.2
XM_017021201.1		Intron			XP_016876690.1
XM_017021202.1		Intron			XP_016876691.1
XM_017021203.1		Intron			XP_016876692.1
XM_017021204.1		Intron			XP_016876693.1
XM_017021205.1		Intron			XP_016876694.1
XM_017021206.1		Intron			XP_016876695.1
XM_017021207.1		Intron			XP_016876696.1
XM_017021208.1		Intron			XP_016876697.1
XM_017021209.1		Intron			XP_016876698.1
XM_017021210.1		Intron			XP_016876699.1
XM_017021211.1		Intron			XP_016876700.1
XM_017021212.1		Intron			XP_016876701.1
XM_017021213.1		Intron			XP_016876702.1
XM_017021214.1		Intron			XP_016876703.1
XM_017021215.1		Intron			XP_016876704.1

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