Product Details

SNP ID
rs74115415
Assay Type
Functionally tested
NCBI dbSNP Submissions
26
Location
Chr.1:153390571 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACTTGCCCCACCTGAAAAACAGAA[C/T]CTTCTGGGGAATCCCATGGCAGGGA
Phenotype
MIM: 123885
Polymorphism
C/T, Transition 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_001319196.1 149 Missense Mutation NP_001306125.1
NM_001319197.1 149 Missense Mutation NP_001306126.1
NM_001319198.1 149 Intron NP_001306127.1
NM_001319201.1 149 Intron NP_001306130.1
NM_002964.4 149 Intron NP_002955.2

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