Product Details

SNP ID
rs4987363
Assay Type
Functionally tested
NCBI dbSNP Submissions
22
Location
Chr.1:169694797 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCTCAGTAATGCTCAATGCTTGGCC[A/G]TCTGACCTCTGTCTTGATGTCTGCA
Phenotype
MIM: 153240
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SELL PubMed Links

Gene Details

Gene
SELL
Gene Name
selectin L
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000655.4 Intron NP_000646.2

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