Product Details

SNP ID
rs12589576
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34518861 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCATGTTCAGTCCATGTGTCCTTA[A/C]AAGTGAAGCAAGTTTCTTCTAGGCA
Phenotype
MIM: 609486
Polymorphism
A/C, Transversion 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_001318916.1 762 Intron NP_001305845.1
NM_018453.3 762 Intron NP_060923.2
XM_011536958.1 762 Intron XP_011535260.1
XM_017021460.1 762 Missense Mutation TGT,TTT C218F XP_016876949.1

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