Product Details

SNP ID

rs201224544

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54631506 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTCCTGATTTCCTTCCAGGGCACC[A/T]CCCCAAGCCCACCCTCTGGGCTGAA

Phenotype

MIM: 604811

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

LILRB1 PubMed Links

Gene Details

Gene

LILRB1

Gene Name

leukocyte immunoglobulin like receptor B1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001081637.2	348	Intron			NP_001075106.2
NM_001081638.3	348	Missense Mutation	CAC,CTC	H26L	NP_001075107.2
NM_001081639.3	348	Missense Mutation	CAC,CTC	H26L	NP_001075108.2
NM_001278398.2	348	Intron			NP_001265327.2
NM_001278399.2	348	Missense Mutation	CAC,CTC	H26L	NP_001265328.2
NM_006669.6	348	Missense Mutation	CAC,CTC	H26L	NP_006660.4
XM_011526331.2	348	Intron			XP_011524633.1
XM_011526332.2	348	Intron			XP_011524634.1
XM_011526335.2	348	Intron			XP_011524637.1
XM_011526336.2	348	Intron			XP_011524638.1
XM_011526338.2	348	Intron			XP_011524640.1
XM_017026182.1	348	Intron			XP_016881671.1
XM_017026183.1	348	Intron			XP_016881672.1
XM_017026184.1	348	Intron			XP_016881673.1
XM_017026185.1	348	Intron			XP_016881674.1
XM_017026186.1	348	Intron			XP_016881675.1
XM_017026187.1	348	Missense Mutation	CAC,CTC	H43L	XP_016881676.1
XM_017026188.1	348	Missense Mutation	CAC,CTC	H43L	XP_016881677.1
XM_017026189.1	348	Missense Mutation	CAC,CTC	H43L	XP_016881678.1
XM_017026190.1	348	Missense Mutation	CAC,CTC	H43L	XP_016881679.1
XM_017026191.1	348	Intron			XP_016881680.1
XM_017026192.1	348	Intron			XP_016881681.1

View Full Product Details