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SNP ID: rs2460827
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:18231629 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGTGCTGCTGTTTCCAAATAAATAG[C/T]AGTCTATTAATCCCTGAAGATAGAC
Phenotype: MIM: 104751 MIM: 104752
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SAA2 PubMed Links

Gene Details

Gene: SAA2
Gene Name: serum amyloid A2

There are no transcripts associated with this gene.

Gene: SAA2-SAA4
Gene Name: SAA2-SAA4 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199744.1	576	Missense Mutation	TAC,TGC	Y167C	NP_001186673.1

Gene: SAA4
Gene Name: serum amyloid A4, constitutive

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006512.3	576	Missense Mutation	TAC,TGC	Y89C	NP_006503.2

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