Product Details

SNP ID

rs17352411

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:34524776 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCACTATTTGGAACAGGCTGTTGTT[C/G]ACGTGATCTCTGTGGTCCCAAACCA

Phenotype

MIM: 609486

Polymorphism

C/G, 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	889	Silent Mutation	GTC,GTG	V128V	NP_001305845.1
NM_018453.3	889	Missense Mutation	CAA,GAA	Q168E	NP_060923.2
XM_011536958.1	889	Missense Mutation	CAA,GAA	Q104E	XP_011535260.1
XM_017021460.1	889	Missense Mutation	CAA,GAA	Q168E	XP_016876949.1

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