Product Details

SNP ID
rs202044660
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34516328 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCTGTTTAGGAATGGCTTGCTAA[A/C]ACATTGAAAAAATGAAAGACTTCAT
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 1227 UTR 3 NP_001305845.1
NM_018453.3 1227 Silent Mutation GTG,GTT V280V NP_060923.2
XM_011536958.1 1227 Silent Mutation GTG,GTT V216V XP_011535260.1
XM_017021460.1 1227 Intron XP_016876949.1

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