Product Details

SNP ID
rs3917459
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:169726674 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAAATGTATTTTCAAAAACATTTTT[A/G]AAGTACATTCATAAACTTCCTCACC
Phenotype
MIM: 131210
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SELE PubMed Links

Gene Details

Gene
SELE
Gene Name
selectin E
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000450.2 Intron NP_000441.2

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