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AGAGGCGCGAGTTGGGGAGTGGGGG[C/T]GGGTGCTCCATGGCCATGGGGGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138321 MIM: 607714 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPX3 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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GPX3 - glutathione peroxidase 3 | ||||||
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There are no transcripts associated with this gene. |
TNIP1 - TNFAIP3 interacting protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252385.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_001239314.1 | |
NM_001252386.1 | 1852 | Silent Mutation | CCA,CCG | P,P 529 | NP_001239315.1 | |
NM_001252390.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_001239319.1 | |
NM_001252391.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_001239320.1 | |
NM_001252392.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_001239321.1 | |
NM_001252393.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_001239322.1 | |
NM_001258454.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_001245383.1 | |
NM_001258455.1 | 1852 | Intron | NP_001245384.1 | |||
NM_001258456.1 | 1852 | Intron | NP_001245385.1 | |||
NM_006058.4 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | NP_006049.3 | |
XM_005268355.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | XP_005268412.1 | |
XM_006714751.1 | 1852 | Intron | XP_006714814.1 | |||
XM_006714752.2 | 1852 | Intron | XP_006714815.1 | |||
XM_017008945.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | XP_016864434.1 | |
XM_017008946.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | XP_016864435.1 | |
XM_017008947.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | XP_016864436.1 | |
XM_017008948.1 | 1852 | Silent Mutation | CCA,CCG | P,P 529 | XP_016864437.1 | |
XM_017008949.1 | 1852 | Intron | XP_016864438.1 | |||
XM_017008950.1 | 1852 | Silent Mutation | CCA,CCG | P,P 582 | XP_016864439.1 | |
XM_017008951.1 | 1852 | Silent Mutation | CCA,CCG | P,P 529 | XP_016864440.1 |