Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAGCCACCCCTCTGGCTGCTCCTG[C/T]GGGTTCCCTGTCCAGGAAGAAGCGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607898 | ||||||||||||||||||||
Literature Links: |
TRIB3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
TRIB3 - tribbles pseudokinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301188.1 | 78 | Missense Mutation | GCG,GTG | A,V 10 | NP_001288117.1 | |
NM_001301190.1 | 78 | Missense Mutation | GCG,GTG | A,V 10 | NP_001288119.1 | |
NM_001301193.1 | 78 | Missense Mutation | GCG,GTG | A,V 10 | NP_001288122.1 | |
NM_001301196.1 | 78 | Missense Mutation | GCG,GTG | A,V 10 | NP_001288125.1 | |
NM_001301201.1 | 78 | Missense Mutation | GCG,GTG | A,V 37 | NP_001288130.1 | |
NM_021158.4 | 78 | Missense Mutation | GCG,GTG | A,V 10 | NP_066981.2 | |
XM_017027989.1 | 78 | Missense Mutation | GCG,GTG | A,V 37 | XP_016883478.1 |