Product Details

SNP ID
rs7142802
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34523680 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCTATCGAGTAGCTGGGTCTACAC[A/G]CATACATCACTATACTCAGCTAATT
Phenotype
MIM: 609486
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EAPP PubMed Links

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 Intron NP_001305845.1
NM_018453.3 Intron NP_060923.2
XM_011536958.1 Intron XP_011535260.1
XM_017021460.1 Intron XP_016876949.1

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