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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