Product Details

SNP ID

rs149923274

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:34516332 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTTAGGAATGGCTTGCTAAAACA[C/T]TGAAAAAATGAAAGACTTCATCCTT

Phenotype

MIM: 609486

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EAPP PubMed Links

Additional Information

For this assay, SNP(s) [rs7766] 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

EAPP

Gene Name

E2F associated phosphoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318916.1	1223	UTR 3			NP_001305845.1
NM_018453.3	1223	Missense Mutation	AAT,AGT	N279S	NP_060923.2
XM_011536958.1	1223	Missense Mutation	AAT,AGT	N215S	XP_011535260.1
XM_017021460.1	1223	Intron			XP_016876949.1

View Full Product Details