Product Details

SNP ID

rs112064008

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:19225735 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAGTGTTTTATGTGCACTCACCTG[C/G]AATTGGGGAGCTGTAAATCCTGTGG

Phenotype

MIM: 612047

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

E2F8 PubMed Links

Additional Information

For this assay, SNP(s) [rs793274] 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

E2F8

Gene Name

E2F transcription factor 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256371.1	2545	Missense Mutation	CCA,GCA	P675A	NP_001243300.1
NM_001256372.1	2545	Missense Mutation	CCA,GCA	P675A	NP_001243301.1
NM_024680.3	2545	Missense Mutation	CCA,GCA	P675A	NP_078956.2
XM_011520367.1	2545	Missense Mutation	CCA,GCA	P570A	XP_011518669.1

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