Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615606 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
BTNL8 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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BTNL8 - butyrophilin like 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040462.2 | 466 | Missense Mutation | ACG,GCG | T,A 143 | NP_001035552.1 | |
NM_001159707.1 | 466 | Missense Mutation | ACG,GCG | T,A 27 | NP_001153179.1 | |
NM_001159708.1 | 466 | Missense Mutation | ACG,GCG | T,A 143 | NP_001153180.1 | |
NM_001159709.1 | 466 | Missense Mutation | ACG,GCG | T,A 18 | NP_001153181.1 | |
NM_001159710.1 | 466 | UTR 5 | NP_001153182.1 | |||
NM_024850.2 | 466 | Missense Mutation | ACG,GCG | T,A 143 | NP_079126.1 | |
XM_011534649.1 | 466 | Missense Mutation | ACG,GCG | T,A 143 | XP_011532951.1 | |
XM_011534650.2 | 466 | Missense Mutation | ACG,GCG | T,A 93 | XP_011532952.1 | |
XM_011534651.2 | 466 | Missense Mutation | ACG,GCG | T,A 32 | XP_011532953.1 | |
XM_011534652.2 | 466 | Missense Mutation | ACG,GCG | T,A 24 | XP_011532954.1 | |
XM_011534653.2 | 466 | Intron | XP_011532955.1 |
Set Membership: |
HapMap Validated |