Product Details

SNP ID
rs61762487
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:108623389 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTGGTCTGGGGCCCCCACTGGGT[G/A]GTTGACGGACAAATTGCTGGCTGCC
Phenotype
MIM: 600738
Polymorphism
G/A, Transition substitution
Allele Nomenclature
Literature Links
SELPLG PubMed Links

Gene Details

Gene
SELPLG
Gene Name
selectin P ligand
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206609.1 1144 Missense Mutation CAC,TAC H323Y NP_001193538.1
NM_003006.4 1144 Missense Mutation CAC,TAC H307Y NP_002997.2

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