Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGAGTACTCAGAAAGTAGAGTCAC[C/T]TGTGCTGCAGGGGCAAGAAGGCATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
TRMT10B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
TRMT10B - tRNA methyltransferase 10B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286950.1 | 150 | Missense Mutation | CCT,CTT | P,L 15 | NP_001273879.1 | |
NM_001286951.1 | 150 | UTR 5 | NP_001273880.1 | |||
NM_001286952.1 | 150 | Missense Mutation | CCT,CTT | P,L 15 | NP_001273881.1 | |
NM_001286953.1 | 150 | UTR 5 | NP_001273882.1 | |||
NM_001286954.1 | 150 | UTR 5 | NP_001273883.1 | |||
NM_144964.3 | 150 | Missense Mutation | CCT,CTT | P,L 15 | NP_659401.2 | |
XM_005251375.2 | 150 | Missense Mutation | CCT,CTT | P,L 15 | XP_005251432.1 | |
XM_005251379.2 | 150 | UTR 5 | XP_005251436.1 | |||
XM_011517735.2 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_011516037.1 | |
XM_011517736.2 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_011516038.1 | |
XM_011517738.2 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_011516040.1 | |
XM_011517739.2 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_011516041.1 | |
XM_011517742.1 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_011516044.1 | |
XM_011517743.2 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_011516045.1 | |
XM_017014313.1 | 150 | Missense Mutation | CCT,CTT | P,L 28 | XP_016869802.1 |