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SNP ID

rs140163350

Assay Type

Functionally tested

NCBI dbSNP Submissions

12

Location

Chr.1:153360639 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCTCACAGCCTTCTCTCCCCACC[C/T]GCAGAAGGAGAATAAGAATGAAAAG

Phenotype

MIM: 123886

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

S100A9 PubMed Links

Gene Details

Gene

S100A9

Gene Name

S100 calcium binding protein A9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002965.3		Intron			NP_002956.1

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