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AGGCCAACGTGGAACCTGTTGTGCC[A/G]TCAGAGGCTTCAGAGCCGGTGCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607917 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SELO PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SELO - selenoprotein O | ||||||
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There are no transcripts associated with this gene. |
TRABD - TraB domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320484.1 | 190 | Silent Mutation | CCA,CCG | P,P 19 | NP_001307413.1 | |
NM_001320485.1 | 190 | Silent Mutation | CCA,CCG | P,P 19 | NP_001307414.1 | |
NM_001320487.1 | 190 | Silent Mutation | CCA,CCG | P,P 19 | NP_001307416.1 | |
NM_001320488.1 | 190 | Silent Mutation | CCA,CCG | P,P 19 | NP_001307417.1 | |
NM_025204.3 | 190 | Silent Mutation | CCA,CCG | P,P 19 | NP_079480.2 | |
XM_006724422.3 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_006724485.1 | |
XM_006724423.3 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_006724486.1 | |
XM_011530712.2 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_011529014.2 | |
XM_011530713.2 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_011529015.2 | |
XM_011530715.2 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_011529017.2 | |
XM_011530716.2 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_011529018.1 | |
XM_011530717.2 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_011529019.1 | |
XM_011530718.2 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_011529020.1 | |
XM_017028943.1 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_016884432.1 | |
XM_017028944.1 | 190 | Silent Mutation | CCA,CCG | P,P 19 | XP_016884433.1 |