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GGTGGCTTTCCACACAGTGCTTCAC[C/G]AGCTCCTGCTGGTCCAGGTTGCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CTU2 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 |
CTU2 - cytosolic thiouridylase subunit 2 | ||||||
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There are no transcripts associated with this gene. |
RNF166 - ring finger protein 166 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171815.1 | 591 | Silent Mutation | CTC,CTG | L,L 84 | NP_001165286.1 | |
NM_001171816.1 | 591 | Silent Mutation | CTC,CTG | L,L 56 | NP_001165287.1 | |
NM_178841.3 | 591 | Silent Mutation | CTC,CTG | L,L 165 | NP_849163.1 | |
XM_011522845.2 | 591 | Missense Mutation | CGT,GGT | R,G 218 | XP_011521147.1 | |
XM_011522846.1 | 591 | Silent Mutation | CTC,CTG | L,L 165 | XP_011521148.1 | |
XM_011522847.1 | 591 | Silent Mutation | CTC,CTG | L,L 56 | XP_011521149.1 | |
XM_017022910.1 | 591 | Missense Mutation | CGT,GGT | R,G 244 | XP_016878399.1 | |
XM_017022911.1 | 591 | Intron | XP_016878400.1 | |||
XM_017022912.1 | 591 | Intron | XP_016878401.1 | |||
XM_017022913.1 | 591 | Silent Mutation | CTC,CTG | L,L 56 | XP_016878402.1 |