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CACACGGCTTCTCCCACTACCTGCT[A/G]TCACACCCCAGTGACCCCCTGGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604821 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LILRB4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LILRB4 - leukocyte immunoglobulin like receptor B4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278426.3 | 857 | Silent Mutation | CTA,CTG | L,L 206 | NP_001265355.2 | |
NM_001278427.3 | 857 | Silent Mutation | CTA,CTG | L,L 206 | NP_001265356.2 | |
NM_001278428.3 | 857 | Silent Mutation | CTA,CTG | L,L 206 | NP_001265357.2 | |
NM_001278429.3 | 857 | Silent Mutation | CTA,CTG | L,L 235 | NP_001265358.2 | |
NM_001278430.3 | 857 | Intron | NP_001265359.2 | |||
XM_017026215.1 | 857 | Silent Mutation | CTA,CTG | L,L 247 | XP_016881704.1 | |
XM_017026216.1 | 857 | Silent Mutation | CTA,CTG | L,L 247 | XP_016881705.1 | |
XM_017026217.1 | 857 | Silent Mutation | CTA,CTG | L,L 247 | XP_016881706.1 |