Product Details

SNP ID: rs143257705
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:70408547 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTCTTTACTTACTGATTTAACTTCC[C/T]CCTCTGACGGTTTGTGTATCTCTAA
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