Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTACAGCTACTGGAGGTAGCGATAG[C/G]CTTTAAAGCAGTGGTTGCCAGCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142290 MIM: 605493 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HPX 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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HPX - hemopexin | ||||||
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There are no transcripts associated with this gene. |
TRIM3 - tripartite motif containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001248006.1 | 2392 | Missense Mutation | GCC,GGC | A,G 739 | NP_001234935.1 | |
NM_001248007.1 | 2392 | Missense Mutation | GCC,GGC | A,G 620 | NP_001234936.1 | |
NM_006458.3 | 2392 | Missense Mutation | GCC,GGC | A,G 739 | NP_006449.2 | |
NM_033278.3 | 2392 | Missense Mutation | GCC,GGC | A,G 739 | NP_150594.2 | |
XM_011519844.1 | 2392 | Missense Mutation | GCC,GGC | A,G 739 | XP_011518146.1 | |
XM_011519845.2 | 2392 | Missense Mutation | GCC,GGC | A,G 620 | XP_011518147.1 | |
XM_017017098.1 | 2392 | Missense Mutation | GCC,GGC | A,G 739 | XP_016872587.1 | |
XM_017017099.1 | 2392 | Missense Mutation | GCC,GGC | A,G 620 | XP_016872588.1 |