Product Details

SNP ID: rs17122060
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:118308327 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGAGGGAATTGGAAGATCCATTGTT[C/T]CCTAAGAGTTGAGGGAAGAGTCCCA
Phenotype: MIM: 186830
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CD3E PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000733.3		Intron			NP_000724.1