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CCTAAAGTATCTGGTTTATTCCCAT[A/C]AAATCTCCACAGAACCTGTTACAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600067 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
UGT2B4 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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UGT2B4 - UDP glucuronosyltransferase family 2 member B4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297615.1 | 1065 | Missense Mutation | NP_001284544.1 | |||
NM_001297616.1 | 1065 | Missense Mutation | NP_001284545.1 | |||
NM_021139.2 | 1065 | Missense Mutation | NP_066962.2 |