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AGCAGGACGAAGGCCACCGAGACCC[C/T]AATCAAAACCTCCAGGTATCTTCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604820 | ||||||||||||||||||||
Literature Links: |
LILRB3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
LILRB3 - leukocyte immunoglobulin like receptor B3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001081450.2 | 1450 | Missense Mutation | AGG,GGG | R,G 447 | NP_001074919.2 | |
NM_001320960.1 | 1450 | Missense Mutation | AGG,GGG | R,G 464 | NP_001307889.1 | |
NM_006864.3 | 1450 | Missense Mutation | AGG,GGG | R,G 447 | NP_006855.3 | |
XM_011526381.2 | 1450 | Intron | XP_011524683.1 | |||
XM_011526382.2 | 1450 | Intron | XP_011524684.1 | |||
XM_017026218.1 | 1450 | Intron | XP_016881707.1 | |||
XM_017026219.1 | 1450 | Intron | XP_016881708.1 | |||
XM_017026220.1 | 1450 | Intron | XP_016881709.1 | |||
XM_017026221.1 | 1450 | Intron | XP_016881710.1 | |||
XM_017026222.1 | 1450 | Intron | XP_016881711.1 | |||
XM_017026223.1 | 1450 | Intron | XP_016881712.1 |