Product Details

SNP ID
rs148227663
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:77024166 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGATGTGTGCGTTGGATGCTCTTG[C/G]GGGTCACTGGAACTGGTGACTGAAA
Phenotype
MIM: 612046
Polymorphism
C/G, 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 2821 Missense Mutation CCC,CGC P862R NP_976328.2
XM_011537966.2 2821 Missense Mutation CCC,CGC P817R XP_011536268.1
XM_011537969.2 2821 Missense Mutation CCC,CGC P761R XP_011536271.1

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