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GTGACTCTGCGTTGGTGAAAGTCAC[A/G]GTGCCCCCTTCATAATCCAGGGCGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600830 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM26 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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TRIM26 - tripartite motif containing 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242783.1 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | NP_001229712.1 | |
NM_003449.4 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | NP_003440.1 | |
XM_005249374.2 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | XP_005249431.1 | |
XM_005249375.2 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | XP_005249432.1 | |
XM_005249376.2 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | XP_005249433.1 | |
XM_005249377.2 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | XP_005249434.1 | |
XM_005249378.2 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | XP_005249435.1 | |
XM_006715180.2 | 1627 | Silent Mutation | ACC,ACT | T,T 499 | XP_006715243.1 | |
XM_011514859.1 | 1627 | Silent Mutation | ACC,ACT | T,T 422 | XP_011513161.1 | |
XM_017011263.1 | 1627 | Silent Mutation | ACC,ACT | T,T 422 | XP_016866752.1 |