Product Details

SNP ID
rs1224442
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:45016292 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACGGAGGAATGCTTCCATTCAGAC[A/G]GCCCCAGTAAGTACACCCTTGCTTC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DBX2 PubMed Links

Gene Details

Gene
DBX2
Gene Name
developing brain homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001004329.2 1186 Silent Mutation GCC,GCT A338A NP_001004329.2

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