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CTCCTTGGGCCACTGCAAATAAGTC[T/C]GCTGCGTCATGAGAGCCTTCAGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605403 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TLR6 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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TLR6 - toll like receptor 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006068.4 | 2379 | Missense Mutation | CAG,CGG | Q,R 758 | NP_006059.2 | |
XM_005262637.4 | 2379 | Missense Mutation | CAG,CGG | Q,R 758 | XP_005262694.1 | |
XM_011513612.2 | 2379 | Missense Mutation | CAG,CGG | Q,R 758 | XP_011511914.1 | |
XM_011513613.2 | 2379 | Missense Mutation | CAG,CGG | Q,R 758 | XP_011511915.1 | |
XM_011513614.2 | 2379 | Missense Mutation | CAG,CGG | Q,R 758 | XP_011511916.1 |