Product Details

SNP ID

rs11963052

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:20360355 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCCAAATTAATAAGTGAAGAAAATT[A/G]TCATCACGCTATTTTATTTTGCATT

Phenotype

MIM: 600427

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

E2F3 PubMed Links

Additional Information

For this assay, SNP(s) [rs144504314] 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

E2F3

Gene Name

E2F transcription factor 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243076.2		Intron			NP_001230005.1
NM_001949.4		Intron			NP_001940.1
XM_005248865.4		Intron			XP_005248922.1
XM_005248866.4		Intron			XP_005248923.1
XM_011514324.2		Intron			XP_011512626.1
XM_011514328.2		Intron			XP_011512630.1
XM_017010330.1		Intron			XP_016865819.1

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