Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611499 MIM: 608838 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GUSB 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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GUSB - glucuronidase beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000181.3 | 1821 | Missense Mutation | CCG,CTG | P,L 649 | NP_000172.2 | |
NM_001284290.1 | 1821 | Missense Mutation | CCG,CTG | P,L 503 | NP_001271219.1 | |
NM_001293104.1 | 1821 | Missense Mutation | CCG,CTG | P,L 459 | NP_001280033.1 | |
NM_001293105.1 | 1821 | Missense Mutation | CCG,CTG | P,L 430 | NP_001280034.1 | |
XM_005250297.3 | 1821 | Missense Mutation | CCG,CTG | P,L 598 | XP_005250354.1 | |
XM_011516113.1 | 1821 | Missense Mutation | CCG,CTG | P,L 482 | XP_011514415.1 | |
XM_011516114.1 | 1821 | Missense Mutation | CCG,CTG | P,L 425 | XP_011514416.1 | |
XM_017012091.1 | 1821 | Missense Mutation | CCG,CTG | P,L 431 | XP_016867580.1 | |
XM_017012092.1 | 1821 | Missense Mutation | CCG,CTG | P,L 408 | XP_016867581.1 | |
XM_017012093.1 | 1821 | Missense Mutation | CCG,CTG | P,L 374 | XP_016867582.1 |
VKORC1L1 - vitamin K epoxide reductase complex subunit 1 like 1 | ||||||
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There are no transcripts associated with this gene. |