Product Details

SNP ID
rs201703551
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:153390136 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGGCTTTCTTCATGGCTTTTTTT[G/T]TGGGCTGCCACGCCCATCTTTATCA
Phenotype
MIM: 123885
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
S100A8 PubMed Links

Gene Details

Gene
S100A8
Gene Name
S100 calcium binding protein A8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001319196.1 391 Missense Mutation CAA,CAC Q107H NP_001306125.1
NM_001319197.1 391 Missense Mutation CAA,CAC Q106H NP_001306126.1
NM_001319198.1 391 Missense Mutation CAA,CAC Q91H NP_001306127.1
NM_001319201.1 391 Missense Mutation CAA,CAC Q83H NP_001306130.1
NM_002964.4 391 Missense Mutation CAA,CAC Q83H NP_002955.2

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