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See other LILRB1 GT Assays ›
SNP ID:
rs201209520
Gene
LILRB1
Gene Name
Set Membership:
-
Chromosome Location:
Chr.19: 54631500 - 54631500 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AATCTGACTCCTGATTTCCTTCCAG[A/G]GCACCTCCCCAAGCCCACCCTCTGG

Assay ID C_190500952_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 604811

Literature Links:

 LILRB1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
LILRB1 - leukocyte immunoglobulin like receptor B1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001081637.2 342 Intron NP_001075106.2
NM_001081638.3 342 Missense Mutation GAG,GGG E,G 24 NP_001075107.2
NM_001081639.3 342 Missense Mutation GAG,GGG E,G 24 NP_001075108.2
NM_001278398.2 342 Intron NP_001265327.2
NM_001278399.2 342 Missense Mutation GAG,GGG E,G 24 NP_001265328.2
NM_006669.6 342 Missense Mutation GAG,GGG E,G 24 NP_006660.4
XM_011526331.2 342 Intron XP_011524633.1
XM_011526332.2 342 Intron XP_011524634.1
XM_011526335.2 342 Intron XP_011524637.1
XM_011526336.2 342 Intron XP_011524638.1
XM_011526338.2 342 Intron XP_011524640.1
XM_017026182.1 342 Intron XP_016881671.1
XM_017026183.1 342 Intron XP_016881672.1
XM_017026184.1 342 Intron XP_016881673.1
XM_017026185.1 342 Intron XP_016881674.1
XM_017026186.1 342 Intron XP_016881675.1
XM_017026187.1 342 Missense Mutation GAG,GGG E,G 41 XP_016881676.1
XM_017026188.1 342 Missense Mutation GAG,GGG E,G 41 XP_016881677.1
XM_017026189.1 342 Missense Mutation GAG,GGG E,G 41 XP_016881678.1
XM_017026190.1 342 Missense Mutation GAG,GGG E,G 41 XP_016881679.1
XM_017026191.1 342 Intron XP_016881680.1
XM_017026192.1 342 Intron XP_016881681.1

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Gene Ontology Categories:

Function(s) Process(es)


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