Product Details

SNP ID

rs61738512

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54631736 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGTATCGCTGTTACTATGGTAGC[C/G]ACACTGCAGGCCGCTCAGAGAGCAG

Phenotype

MIM: 604811

Polymorphism

C/G, 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	578	Intron			NP_001075106.2
NM_001081638.3	578	Missense Mutation	CAC,GAC	H103D	NP_001075107.2
NM_001081639.3	578	Missense Mutation	CAC,GAC	H103D	NP_001075108.2
NM_001278398.2	578	Intron			NP_001265327.2
NM_001278399.2	578	Missense Mutation	CAC,GAC	H103D	NP_001265328.2
NM_006669.6	578	Missense Mutation	CAC,GAC	H103D	NP_006660.4
XM_011526331.2	578	Intron			XP_011524633.1
XM_011526332.2	578	Intron			XP_011524634.1
XM_011526335.2	578	Intron			XP_011524637.1
XM_011526336.2	578	Intron			XP_011524638.1
XM_011526338.2	578	Intron			XP_011524640.1
XM_017026182.1	578	Intron			XP_016881671.1
XM_017026183.1	578	Intron			XP_016881672.1
XM_017026184.1	578	Intron			XP_016881673.1
XM_017026185.1	578	Intron			XP_016881674.1
XM_017026186.1	578	Intron			XP_016881675.1
XM_017026187.1	578	Missense Mutation	CAC,GAC	H120D	XP_016881676.1
XM_017026188.1	578	Missense Mutation	CAC,GAC	H120D	XP_016881677.1
XM_017026189.1	578	Missense Mutation	CAC,GAC	H120D	XP_016881678.1
XM_017026190.1	578	Missense Mutation	CAC,GAC	H120D	XP_016881679.1
XM_017026191.1	578	Intron			XP_016881680.1
XM_017026192.1	578	Intron			XP_016881681.1

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