Product Details

SNP ID

rs141743480

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:77024180 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATGCTCTTGGGGGTCACTGGAAC[G/T]GGTGACTGAAAAAAGAAAAAAGAAA

Phenotype

MIM: 612046

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

E2F7 PubMed Links

Gene Details

Gene

E2F7

Gene Name

E2F transcription factor 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203394.2	2807	Silent Mutation	CCA,CCC	P857P	NP_976328.2
XM_011537966.2	2807	Silent Mutation	CCA,CCC	P812P	XP_011536268.1
XM_011537969.2	2807	Silent Mutation	CCA,CCC	P756P	XP_011536271.1

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