Product Details

SNP ID
rs150387289
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:19225453 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGGTGAAGTTTACAATGGCTGAG[C/G]TTGGGTTCTGGATGGGAACAGGGTG
Phenotype
MIM: 612047
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
E2F8 PubMed Links

Gene Details

Gene
E2F8
Gene Name
E2F transcription factor 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256371.1 2711 Missense Mutation ACC,AGC T730S NP_001243300.1
NM_001256372.1 2711 Missense Mutation ACC,AGC T730S NP_001243301.1
NM_024680.3 2711 Missense Mutation ACC,AGC T730S NP_078956.2
XM_011520367.1 2711 Missense Mutation ACC,AGC T625S XP_011518669.1

View Full Product Details