Product Details

SNP ID
rs150255844
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:19224693 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTCTGTTGAGACTTCCAGTTTTC[A/G]CTGTGGGACAAAGAGAGTTCCTAAG
Phenotype
MIM: 612047
Polymorphism
A/G, Transition 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 3091 Nonsense Mutation CGA,TGA R857* NP_001243300.1
NM_001256372.1 3091 Nonsense Mutation CGA,TGA R857* NP_001243301.1
NM_024680.3 3091 Nonsense Mutation CGA,TGA R857* NP_078956.2
XM_011520367.1 3091 Nonsense Mutation CGA,TGA R752* XP_011518669.1

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