Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300697 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HUWE1 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)
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EUR
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AMR
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HUWE1 - HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031407.6 | 15665 | Silent Mutation | ACC,ACG | T,T 4090 | NP_113584.3 | |
XM_005261965.3 | 15665 | Silent Mutation | ACC,ACG | T,T 4090 | XP_005262022.1 | |
XM_011530747.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4173 | XP_011529049.1 | |
XM_011530751.2 | 15665 | Silent Mutation | ACC,ACG | T,T 4173 | XP_011529053.1 | |
XM_017029191.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4217 | XP_016884680.1 | |
XM_017029192.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4216 | XP_016884681.1 | |
XM_017029193.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4210 | XP_016884682.1 | |
XM_017029194.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4202 | XP_016884683.1 | |
XM_017029195.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4201 | XP_016884684.1 | |
XM_017029196.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4200 | XP_016884685.1 | |
XM_017029197.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4184 | XP_016884686.1 | |
XM_017029198.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4180 | XP_016884687.1 | |
XM_017029199.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4180 | XP_016884688.1 | |
XM_017029200.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4180 | XP_016884689.1 | |
XM_017029201.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4180 | XP_016884690.1 | |
XM_017029202.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4180 | XP_016884691.1 | |
XM_017029203.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4180 | XP_016884692.1 | |
XM_017029204.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4134 | XP_016884693.1 | |
XM_017029205.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4093 | XP_016884694.1 | |
XM_017029206.1 | 15665 | Silent Mutation | ACC,ACG | T,T 4083 | XP_016884695.1 |
Set Membership: |
HapMap |