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CAGCATGCCTTGAAGCACTATCTGA[C/T]GCCAAGATCTGAACCTCACTGTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604735 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
USP16 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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USP16 - ubiquitin specific peptidase 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001992.1 | 493 | Missense Mutation | ACG,ATG | T,M 97 | NP_001001992.1 | |
NM_001032410.1 | 493 | Missense Mutation | ACG,ATG | T,M 97 | NP_001027582.1 | |
NM_006447.2 | 493 | Missense Mutation | ACG,ATG | T,M 97 | NP_006438.1 | |
XM_017028257.1 | 493 | Missense Mutation | ACG,ATG | T,M 97 | XP_016883746.1 | |
XM_017028258.1 | 493 | Missense Mutation | ACG,ATG | T,M 97 | XP_016883747.1 | |
XM_017028259.1 | 493 | Missense Mutation | ACG,ATG | T,M 97 | XP_016883748.1 | |
XM_017028260.1 | 493 | UTR 5 | XP_016883749.1 | |||
XM_017028261.1 | 493 | UTR 5 | XP_016883750.1 |