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TGTACTGCGTGAGCTGTCGAACCCC[A/G]GTGTGTTATCTGTGCCTGGAGGAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 610584 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM67 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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TRIM67 - tripartite motif containing 67 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004342.3 | 819 | Silent Mutation | CCA,CCG | P,P 321 | NP_001004342.3 | |
NM_001300889.1 | 819 | Silent Mutation | CCA,CCG | P,P 259 | NP_001287818.1 | |
XM_011544192.2 | 819 | Silent Mutation | CCA,CCG | P,P 321 | XP_011542494.1 | |
XM_017001323.1 | 819 | Silent Mutation | CCA,CCG | P,P 321 | XP_016856812.1 |