Product Details

SNP ID
rs12464355
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:118092274 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTGTCTACTGGGATCTGGGGAAGT[A/G]AAGAGTCAACTAATGTTCTTATACA
Phenotype
MIM: 608660
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
INSIG2 PubMed Links

Gene Details

Gene
INSIG2
Gene Name
insulin induced gene 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321329.1 Intron NP_001308258.1
NM_001321330.1 Intron NP_001308259.1
NM_001321331.1 Intron NP_001308260.1
NM_001321332.1 Intron NP_001308261.1
NM_001321333.1 Intron NP_001308262.1
NM_016133.3 Intron NP_057217.2

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