Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603591 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
USP13 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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Japanese
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CHB (Han Chinese) - Not Available | ||||||
AFR
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Chinese
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JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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USP13 - ubiquitin specific peptidase 13 (isopeptidase T-3) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003940.2 | 169 | Silent Mutation | AAC,AAT | N,N 47 | NP_003931.2 | |
XM_011513269.1 | 169 | Missense Mutation | AAC,AAT | N,N 47 | XP_011511571.1 | |
XM_017007425.1 | 169 | Intron | XP_016862914.1 | |||
XM_017007426.1 | 169 | Silent Mutation | AAC,AAT | N,N 47 | XP_016862915.1 | |
XM_017007427.1 | 169 | Intron | XP_016862916.1 |
Set Membership: |
Validated |