Product Details

SNP ID

rs138910107

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:127692221 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCAGGGTGGGGACGCAGTTCCTG[C/T]CGTGGCTGTCCTTTGAGAGACCCAC

Phenotype

MIM: 609699

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MGLL PubMed Links

Gene Details

Gene

MGLL

Gene Name

monoglyceride lipase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003794.2	1206	Missense Mutation	ACA,GCA	T297A	NP_001003794.1
NM_001256585.1	1206	Missense Mutation	ACA,GCA	T277A	NP_001243514.1
NM_007283.6	1206	Missense Mutation	ACA,GCA	T307A	NP_009214.1
XM_011512377.1	1206	Missense Mutation	ACA,GCA	T333A	XP_011510679.1
XM_011512378.1	1206	Missense Mutation	ACA,GCA	T323A	XP_011510680.1
XM_011512379.2	1206	Missense Mutation	ACA,GCA	T297A	XP_011510681.1
XM_011512382.1	1206	Missense Mutation	ACA,GCA	T260A	XP_011510684.1
XM_011512383.2	1206	Missense Mutation	ACA,GCA	T241A	XP_011510685.1
XM_017005662.1	1206	Intron			XP_016861151.1
XM_017005663.1	1206	Intron			XP_016861152.1
XM_017005664.1	1206	Missense Mutation	ACA,GCA	T271A	XP_016861153.1
XM_017005665.1	1206	Missense Mutation	ACA,GCA	T271A	XP_016861154.1
XM_017005666.1	1206	Missense Mutation	ACA,GCA	T267A	XP_016861155.1

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