Product Details

SNP ID: rs114522590
Assay Type: Functionally tested
NCBI dbSNP Submissions: 8
Location: Chr.1:153373950 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCCTTGGAATATTTCATCAATGAC[A/G]GCTTTATCTTTGATATTCTAGGAAA
Phenotype: MIM: 603112
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: S100A12 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005621.1	224	Silent Mutation	GCC,GCT	A52A	NP_005612.1