Product Details

SNP ID
rs1629534
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:1809481 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGGCGACTCGTGCTGGCCGAGCCC[A/C]GCCCTCAGAGGACACGGAGGGCGGG
Phenotype
MIM: 138760
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
HAGH PubMed Links
Additional Information
For this assay, SNP(s) [rs118097552] are located under a probe 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
HAGH
Gene Name
hydroxyacylglutathione hydrolase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040427.1 Intron NP_001035517.1
NM_001286249.1 Intron NP_001273178.1
NM_005326.4 Intron NP_005317.2
XM_011522469.2 Intron XP_011520771.1
XM_011522470.2 Intron XP_011520772.1
XM_017023195.1 Intron XP_016878684.1

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