Product Details

SNP ID

rs143906646

Assay Type

Functionally tested

NCBI dbSNP Submissions

16

Location

Chr.1:153360788 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACGAGAAGATGCACGAGGGTGAC[A/G]AGGGCCCTGGCCACCACCATAAGCC

Phenotype

MIM: 123886

Polymorphism

A/G, 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	338	Missense Mutation	AAG,GAG	K99E	NP_002956.1

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