Product Details

SNP ID

rs782444

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:127691098 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACACTCCCAGGGTAGCTCTGGGCCA[C/T]AGGCAGGCCCAGGCCCAGGCCTAGG

Phenotype

MIM: 609699

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MGLL PubMed Links

Additional Information

For this assay, SNP(s) [rs76891800] 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

MGLL

Gene Name

monoglyceride lipase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003794.2	2329	UTR 3			NP_001003794.1
NM_001256585.1	2329	UTR 3			NP_001243514.1
NM_007283.6	2329	UTR 3			NP_009214.1
XM_011512377.1	2329	UTR 3			XP_011510679.1
XM_011512378.1	2329	UTR 3			XP_011510680.1
XM_011512379.2	2329	UTR 3			XP_011510681.1
XM_011512382.1	2329	UTR 3			XP_011510684.1
XM_011512383.2	2329	UTR 3			XP_011510685.1
XM_017005662.1	2329	Intron			XP_016861151.1
XM_017005663.1	2329	Intron			XP_016861152.1
XM_017005664.1	2329	UTR 3			XP_016861153.1
XM_017005665.1	2329	UTR 3			XP_016861154.1
XM_017005666.1	2329	UTR 3			XP_016861155.1

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