Product Details

SNP ID
rs144988471
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34516346 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCTAAAACATTGAAAAAATGAAA[G/T]ACTTCATCCTTGTCGTAGACTGCCA
Phenotype
MIM: 609486
Polymorphism
G/T, 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 1209 UTR 3 NP_001305845.1
NM_018453.3 1209 Silent Mutation GTA,GTC V274V NP_060923.2
XM_011536958.1 1209 Silent Mutation GTA,GTC V210V XP_011535260.1
XM_017021460.1 1209 Intron XP_016876949.1

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