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GCTTTGGCTCCGCATGAGGGAGGGA[C/T]AGCCTGGGAAGACAAGAGATTCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610658 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM29 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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TRIM29 - tripartite motif containing 29 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012101.3 | 1088 | Missense Mutation | TAT,TGT | Y,C 544 | NP_036233.2 | |
XM_005271490.1 | 1088 | Missense Mutation | TAT,TGT | Y,C 277 | XP_005271547.1 | |
XM_011542729.1 | 1088 | Missense Mutation | TAT,TGT | Y,C 578 | XP_011541031.1 | |
XM_011542732.1 | 1088 | Missense Mutation | TAT,TGT | Y,C 577 | XP_011541034.1 | |
XM_011542733.1 | 1088 | Missense Mutation | TAT,TGT | Y,C 311 | XP_011541035.1 | |
XM_017017453.1 | 1088 | Missense Mutation | TAT,TGT | Y,C 317 | XP_016872942.1 | |
XM_017017454.1 | 1088 | Missense Mutation | TAT,TGT | Y,C 283 | XP_016872943.1 |