Product Details

SNP ID
rs1800017
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:169726763 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTAATGTCAGGAGGGAGAGTCCAGC[A/G]GCAGAAAGTCCAGCTACCAAGGGAA
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 1846 Silent Mutation GCC,GCT A563A NP_000441.2

View Full Product Details