Product Details

SNP ID

rs202170300

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54218831 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCAGGACGCTGGAAATCAGTCTT[A/T]CTCTGGTCTGGGTGAAGATGGACAG

Phenotype

MIM: 604820

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

LILRB3 PubMed Links

Additional Information

For this assay, SNP(s) [rs3852891,rs3852892] 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

LILRB3

Gene Name

leukocyte immunoglobulin like receptor B3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001081450.2	1545	Missense Mutation	AGA,AGT	R478S	NP_001074919.2
NM_001320960.1	1545	Missense Mutation	AGA,AGT	R495S	NP_001307889.1
NM_006864.3	1545	Missense Mutation	AGA,AGT	R478S	NP_006855.3
XM_011526381.2	1545	Intron			XP_011524683.1
XM_011526382.2	1545	Intron			XP_011524684.1
XM_017026218.1	1545	Intron			XP_016881707.1
XM_017026219.1	1545	Intron			XP_016881708.1
XM_017026220.1	1545	Intron			XP_016881709.1
XM_017026221.1	1545	Intron			XP_016881710.1
XM_017026222.1	1545	Intron			XP_016881711.1
XM_017026223.1	1545	Intron			XP_016881712.1

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