Product Details

SNP ID

rs9991142

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:69066869 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAAAATGACAGCTCATTTTCATGA[C/T]GATCTCCTGCATTTTCTATGGGAGT

Phenotype

MIM: 600068

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

UGT2B7 PubMed Links

Additional Information

For this assay, SNP(s) [rs77802598] 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

UGT2B7

Gene Name

UDP glucuronosyltransferase family 2 member B7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005265702.3		Intron			XP_005265759.1
XM_011532229.2		Intron			XP_011530531.1
XM_011532230.1		Intron			XP_011530532.1

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