Product Details

SNP ID: rs11597457
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:70418155 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGACCCTCATGATGGGATTTGTGCC[C/T]TTATAAGATGGAACACCACAGAGTT
Phenotype: MIM: 602224
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: EIF4EBP2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004096.4		Intron			NP_004087.1