Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCTGTGGTGATGCACCTCGGGATC[C/T]GCTCTGCCCGCTGTGTCCTGGGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
THEMIS2 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
|
THEMIS2 - thymocyte selection associated family member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039477.2 | 453 | Intron | NP_001034566.1 | |||
NM_001105556.2 | 453 | Missense Mutation | CGC,TGC | R,C 142 | NP_001099026.1 | |
NM_001286113.1 | 453 | Missense Mutation | CGC,TGC | R,C 142 | NP_001273042.1 | |
NM_001286115.1 | 453 | Missense Mutation | CGC,TGC | R,C 142 | NP_001273044.1 | |
NM_004848.3 | 453 | Missense Mutation | CGC,TGC | R,C 142 | NP_004839.2 | |
XM_005246041.3 | 453 | Intron | XP_005246098.1 | |||
XM_006711050.1 | 453 | Missense Mutation | CGC,TGC | R,C 142 | XP_006711113.1 | |
XM_011542445.2 | 453 | Missense Mutation | CGC,TGC | R,C 95 | XP_011540747.1 |