Product Details

SNP ID
rs61734491
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:54218799 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCCCTGTCCTTGGGCTCTGTCTCC[A/G]CAGCCCCTGCAGGACGCTGGAAATC
Phenotype
MIM: 604820
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LILRB3 PubMed Links

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 1577 Missense Mutation NP_001074919.2
NM_001320960.1 1577 Missense Mutation NP_001307889.1
NM_006864.3 1577 Missense Mutation NP_006855.3
XM_011526381.2 1577 Intron XP_011524683.1
XM_011526382.2 1577 Intron XP_011524684.1
XM_017026218.1 1577 Intron XP_016881707.1
XM_017026219.1 1577 Intron XP_016881708.1
XM_017026220.1 1577 Intron XP_016881709.1
XM_017026221.1 1577 Intron XP_016881710.1
XM_017026222.1 1577 Intron XP_016881711.1
XM_017026223.1 1577 Intron XP_016881712.1

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