Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606252 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HP11014 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
|
HP11014 - uncharacterized HP11014 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
TIRAP - TIR domain containing adaptor protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039661.1 | 206 | Missense Mutation | CCT,GCT | P,A 9 | NP_001034750.1 | |
NM_001318776.1 | 206 | Missense Mutation | CCT,GCT | P,A 9 | NP_001305705.1 | |
NM_001318777.1 | 206 | Missense Mutation | CCT,GCT | P,A 9 | NP_001305706.1 | |
NM_148910.2 | 206 | Missense Mutation | CCT,GCT | P,A 9 | NP_683708.1 | |
XM_005271399.3 | 206 | Missense Mutation | CCT,GCT | P,A 9 | XP_005271456.2 | |
XM_011542576.2 | 206 | Missense Mutation | CCT,GCT | P,A 9 | XP_011540878.1 | |
XM_017017161.1 | 206 | Intron | XP_016872650.1 | |||
XM_017017162.1 | 206 | Missense Mutation | CCT,GCT | P,A 9 | XP_016872651.1 |