Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAAGTGGGATTTGGATTTTATGTGC[A/G]CTGATAAGACAAAATCAAACCAAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIT1 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
|
TRIT1 - tRNA isopentenyltransferase 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001312691.1 | 1177 | Missense Mutation | GCG,GTG | A,V 386 | NP_001299620.1 | |
NM_001312692.1 | 1177 | Missense Mutation | GCG,GTG | A,V 330 | NP_001299621.1 | |
NM_017646.5 | 1177 | Missense Mutation | GCG,GTG | A,V 412 | NP_060116.2 | |
XM_005270954.2 | 1177 | Missense Mutation | GCG,GTG | A,V 331 | XP_005271011.1 | |
XM_006710706.1 | 1177 | Missense Mutation | GCG,GTG | A,V 271 | XP_006710769.1 |