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SNP ID: rs12282742
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:18244252 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACATTTTGGCAAGATACAGTTCACT[C/T]CAGAGCACTGCCACTTCCACAGCTG
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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127380.2		Intron			NP_001120852.1
NM_030754.4		Intron			NP_110381.2

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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199744.1		Intron			NP_001186673.1

Gene: SAA4
Gene Name: serum amyloid A4, constitutive

There are no transcripts associated with this gene.

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