Product Details

SNP ID
rs17220479
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:32973038 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGGCCCCGGCGCGCTGCTGTTGCGG[C/T]GCAGCTGTCGACTCGGTCGCGCGGA
Phenotype
MIM: 601540
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BRD2 PubMed Links

Gene Details

Gene
BRD2
Gene Name
bromodomain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001113182.2 Intron NP_001106653.1
NM_001199455.1 Intron NP_001186384.1
NM_001199456.1 Intron NP_001186385.1
NM_001291986.1 Intron NP_001278915.1
NM_005104.3 Intron NP_005095.1

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