Product Details

SNP ID
rs139987242
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:153390418 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCTGATATACTGAGGACACTCGG[C/T]CTCTAGCAATTTCTTCAGGTCATCC
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_001319196.1 260 Missense Mutation ACC,GCC T64A NP_001306125.1
NM_001319197.1 260 Missense Mutation ACC,GCC T63A NP_001306126.1
NM_001319198.1 260 Missense Mutation ACC,GCC T48A NP_001306127.1
NM_001319201.1 260 Missense Mutation ACC,GCC T40A NP_001306130.1
NM_002964.4 260 Missense Mutation ACC,GCC T40A NP_002955.2

View Full Product Details