Product Details

SNP ID
rs748799940
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:153390506 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTGTGGTAGACGTCGATGATAGA[G/T]TTCAAGGCTTTCTCCAGCTCGGTCA
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_001319196.1 172 Missense Mutation AAA,AAC K34N NP_001306125.1
NM_001319197.1 172 Missense Mutation AAA,AAC K33N NP_001306126.1
NM_001319198.1 172 Missense Mutation AAA,AAC K18N NP_001306127.1
NM_001319201.1 172 Missense Mutation AAA,AAC K10N NP_001306130.1
NM_002964.4 172 Missense Mutation AAA,AAC K10N NP_002955.2

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