Product Details

SNP ID

rs3218206

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:23510273 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTCTCCTTAGCCTGGGTGGACTGT[C/T]GTGCTCTCAAAATCCACCTTCCAGA

Phenotype

MIM: 600426

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

E2F2 PubMed Links

Gene Details

Gene

E2F2

Gene Name

E2F transcription factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004091.3		Intron			NP_004082.1
XM_005245748.3		Intron			XP_005245805.1
XM_005245749.3		Intron			XP_005245806.1
XM_011540868.2		Intron			XP_011539170.1
XM_011540870.2		Intron			XP_011539172.1
XM_011540871.2		Intron			XP_011539173.1

View Full Product Details