Product Details

SNP ID

rs2233868

Assay Type

Functionally tested

NCBI dbSNP Submissions

20

Location

Chr.1:153563870 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCCAGCGCCTGCTCCAGAGAACTG[C/G]ACATCATGGATCTGTGGCTGCAGAG

Phenotype

MIM: 176993

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

S100A2 PubMed Links

Gene Details

Gene

S100A2

Gene Name

S100 calcium binding protein A2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005978.3	343	Missense Mutation	TCC,TGC	S2C	NP_005969.1

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