Product Details

SNP ID
rs187250799
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:47218741 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTATAGGGCTCCAGAAGCCAGAGT[A/G]GAAAAAAAAAAAAAAAGAATGTATG
Phenotype
MIM: 600811
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
DDB2 PubMed Links

Gene Details

Gene
DDB2
Gene Name
damage specific DNA binding protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000107.2 Intron NP_000098.1
NM_001300734.1 Intron NP_001287663.1

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