Product Details

SNP ID

rs148337173

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:19225740 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTTATGTGCACTCACCTGCAATT[C/G]GGGAGCTGTAAATCCTGTGGTTTGG

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	2540	Missense Mutation	CCA,CGA	P673R	NP_001243300.1
NM_001256372.1	2540	Missense Mutation	CCA,CGA	P673R	NP_001243301.1
NM_024680.3	2540	Missense Mutation	CCA,CGA	P673R	NP_078956.2
XM_011520367.1	2540	Missense Mutation	CCA,CGA	P568R	XP_011518669.1

View Full Product Details