Product Details

SNP ID

rs201209520

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54631500 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCTGACTCCTGATTTCCTTCCAG[A/G]GCACCTCCCCAAGCCCACCCTCTGG

Phenotype

MIM: 604811

Polymorphism

A/G, Transition 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	342	Intron			NP_001075106.2
NM_001081638.3	342	Missense Mutation	GAG,GGG	E24G	NP_001075107.2
NM_001081639.3	342	Missense Mutation	GAG,GGG	E24G	NP_001075108.2
NM_001278398.2	342	Intron			NP_001265327.2
NM_001278399.2	342	Missense Mutation	GAG,GGG	E24G	NP_001265328.2
NM_006669.6	342	Missense Mutation	GAG,GGG	E24G	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	E41G	XP_016881676.1
XM_017026188.1	342	Missense Mutation	GAG,GGG	E41G	XP_016881677.1
XM_017026189.1	342	Missense Mutation	GAG,GGG	E41G	XP_016881678.1
XM_017026190.1	342	Missense Mutation	GAG,GGG	E41G	XP_016881679.1
XM_017026191.1	342	Intron			XP_016881680.1
XM_017026192.1	342	Intron			XP_016881681.1

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