Product Details

SNP ID

rs310833

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:77024996 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGACTCATTAACTTATATTGATAA[C/T]GTATCTTTGTGTATATTTGTATGTT

Phenotype

MIM: 612046

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

E2F7 PubMed Links

Additional Information

For this assay, SNP(s) [rs115709397] 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

E2F7

Gene Name

E2F transcription factor 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203394.2		Intron			NP_976328.2
XM_011537966.2		Intron			XP_011536268.1
XM_011537969.2		Intron			XP_011536271.1

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