Product Details

SNP ID

rs143837742

Assay Type

Functionally Tested

NCBI dbSNP Submissions

14

Location

Chr.1:81307179 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACAGAAAAGTTTAATGTAGCAAGG[A/C]TTTAAAAAACCTGAATGTTTGTATA

Phenotype

MIM: 607018

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ADGRL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs376151440] 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

ADGRL2

Gene Name

adhesion G protein-coupled receptor L2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001297704.1		Intron			NP_001284633.1
NM_001297705.1		Intron			NP_001284634.1
NM_001297706.1		Intron			NP_001284635.1
NM_012302.3		Intron			NP_036434.1
XM_005270666.4		Intron			XP_005270723.1
XM_005270668.2		Intron			XP_005270725.1
XM_006710485.3		Intron			XP_006710548.1
XM_006710488.2		Intron			XP_006710551.1
XM_006710489.3		Intron			XP_006710552.1
XM_017000782.1		Intron			XP_016856271.1
XM_017000783.1		Intron			XP_016856272.1
XM_017000784.1		Intron			XP_016856273.1
XM_017000785.1		Intron			XP_016856274.1
XM_017000786.1		Intron			XP_016856275.1
XM_017000787.1		Intron			XP_016856276.1
XM_017000788.1		Intron			XP_016856277.1
XM_017000789.1		Intron			XP_016856278.1
XM_017000790.1		Intron			XP_016856279.1
XM_017000791.1		Intron			XP_016856280.1
XM_017000792.1		Intron			XP_016856281.1
XM_017000793.1		Intron			XP_016856282.1
XM_017000794.1		Intron			XP_016856283.1
XM_017000795.1		Intron			XP_016856284.1
XM_017000796.1		Intron			XP_016856285.1
XM_017000797.1		Intron			XP_016856286.1
XM_017000798.1		Intron			XP_016856287.1

View Full Product Details