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TGTGCAGGTGGGACCCATCGCTTAC[A/G]CTGTAGAAGGACACTTCCCCGGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 607868 MIM: 606123 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM11 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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TRIM11 - tripartite motif containing 11 | ||||||
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There are no transcripts associated with this gene. |
TRIM17 - tripartite motif containing 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024940.2 | 2216 | Silent Mutation | AGC,AGT | S,S 433 | NP_001020111.1 | |
NM_001134855.1 | 2216 | Intron | NP_001128327.1 | |||
NM_016102.3 | 2216 | Silent Mutation | AGC,AGT | S,S 433 | NP_057186.1 | |
XM_006711779.2 | 2216 | Silent Mutation | AGC,AGT | S,S 433 | XP_006711842.1 | |
XM_011544209.2 | 2216 | Silent Mutation | AGC,AGT | S,S 433 | XP_011542511.1 | |
XM_011544210.2 | 2216 | Silent Mutation | AGC,AGT | S,S 433 | XP_011542512.1 | |
XM_011544211.2 | 2216 | Silent Mutation | AGC,AGT | S,S 406 | XP_011542513.1 | |
XM_017001418.1 | 2216 | UTR 3 | XP_016856907.1 | |||
XM_017001419.1 | 2216 | UTR 3 | XP_016856908.1 |