Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGCCCAGAAAAGCCCACATTTAC[A/G]CCTATCCTTGGGCCATTCCAAGTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606270 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TLR10 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
TLR10 - toll like receptor 10 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017388.2 | 2416 | Missense Mutation | CGT,TGT | R,C 762 | NP_001017388.1 | |
NM_001195106.1 | 2416 | Missense Mutation | CGT,TGT | R,C 762 | NP_001182035.1 | |
NM_001195107.1 | 2416 | Missense Mutation | CGT,TGT | R,C 762 | NP_001182036.1 | |
NM_001195108.1 | 2416 | Missense Mutation | CGT,TGT | R,C 748 | NP_001182037.1 | |
NM_030956.3 | 2416 | Missense Mutation | CGT,TGT | R,C 762 | NP_112218.2 | |
XM_011513760.2 | 2416 | Missense Mutation | CGT,TGT | R,C 748 | XP_011512062.1 | |
XM_011513761.2 | 2416 | Missense Mutation | CGT,TGT | R,C 762 | XP_011512063.1 | |
XM_011513762.2 | 2416 | Missense Mutation | CGT,TGT | R,C 762 | XP_011512064.1 |