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ATGCGCAAAGGCTCTGGAGGCCCGG[C/T]GCCCCGTGCACCCCCCAGGTAGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 617007 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM35 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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TRIM35 - tripartite motif containing 35 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304495.1 | 1526 | UTR 3 | NP_001291424.1 | |||
NM_171982.4 | 1526 | Missense Mutation | ACC,GCC | T,A 472 | NP_741983.2 | |
XM_005273452.3 | 1526 | UTR 3 | XP_005273509.1 | |||
XM_011544453.1 | 1526 | Missense Mutation | ACC,GCC | T,A 322 | XP_011542755.1 |