Product Details

SNP ID
rs7958377
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.12:77022187 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GCATGGTAGAATTAACATGCATATA[C/T]CCTGCACAGATTGAAACCTGAAAAA
Phenotype
MIM: 612046
Polymorphism
C/T, Transition 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 4800 UTR 3 NP_976328.2
XM_011537966.2 4800 UTR 3 XP_011536268.1
XM_011537969.2 4800 UTR 3 XP_011536271.1

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