Product Details

SNP ID

rs146935882

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54574418 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGAGGAGTACCATCTATATAGGG[A/G]AAACAAATCAGCATCCTGGGTTAGA

Phenotype

MIM: 604812

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LILRA2 PubMed Links

Additional Information

For this assay, SNP(s) [rs533071991] 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

LILRA2

Gene Name

leukocyte immunoglobulin like receptor A2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130917.2	772	Missense Mutation	GAA,GGA	E63G	NP_001124389.2
NM_001290270.1	772	Missense Mutation	GAA,GGA	E51G	NP_001277199.1
NM_001290271.1	772	Missense Mutation	GAA,GGA	E63G	NP_001277200.1
NM_006866.3	772	Missense Mutation	GAA,GGA	E63G	NP_006857.2
XM_006722986.1	772	Missense Mutation	GAA,GGA	E63G	XP_006723049.1
XM_011526385.1	772	Missense Mutation	GAA,GGA	E63G	XP_011524687.1
XM_011526386.1	772	Missense Mutation	GAA,GGA	E51G	XP_011524688.1
XM_011526387.1	772	Missense Mutation	GAA,GGA	E51G	XP_011524689.1
XM_011526388.1	772	Missense Mutation	GAA,GGA	E51G	XP_011524690.1
XM_011526389.1	772	Intron			XP_011524691.1
XM_011526390.1	772	Missense Mutation	GAA,GGA	E63G	XP_011524692.1
XM_011526391.1	772	Missense Mutation	GAA,GGA	E63G	XP_011524693.1
XM_017026224.1	772	Missense Mutation	GAA,GGA	E63G	XP_016881713.1

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