Product Details

SNP ID
rs148686373
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:159066057 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTCAGCATCTAACACACGTGAGGC[A/G]CTATTTACCTCTAAGAAACCACTGT
Phenotype
MIM: 604578
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
AIM2 PubMed Links

Gene Details

Gene
AIM2
Gene Name
absent in melanoma 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004833.1 914 Silent Mutation AGC,AGT S223S NP_004824.1
XM_005245616.4 914 Silent Mutation AGC,AGT S118S XP_005245673.1
XM_017002848.1 914 Silent Mutation AGC,AGT S223S XP_016858337.1

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