Product Details

SNP ID

rs116409526

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:32970533 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTCCGGGGCGAGGGGGAATCTTA[C/T]CGTATATTTGTTCACCTACGTTGAT

Phenotype

MIM: 601540

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

BRD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs150896009] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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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