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TTTCTTTATCTCTTTCCATGTAGTC[C/T]CGGTCAATTAAAGATTCTATTCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300304 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CUL4B 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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CUL4B - cullin 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079872.1 | 2958 | Silent Mutation | CGA,CGG | R,R 878 | NP_001073341.1 | |
NM_003588.3 | 2958 | Silent Mutation | CGA,CGG | R,R 896 | NP_003579.3 | |
XM_005262481.1 | 2958 | Silent Mutation | CGA,CGG | R,R 898 | XP_005262538.1 | |
XM_006724784.1 | 2958 | Silent Mutation | CGA,CGG | R,R 885 | XP_006724847.1 | |
XM_006724785.2 | 2958 | Silent Mutation | CGA,CGG | R,R 883 | XP_006724848.1 | |
XM_011531399.2 | 2958 | Silent Mutation | CGA,CGG | R,R 702 | XP_011529701.1 | |
XM_011531400.2 | 2958 | Silent Mutation | CGA,CGG | R,R 700 | XP_011529702.1 | |
XM_011531401.1 | 2958 | Silent Mutation | CGA,CGG | R,R 684 | XP_011529703.1 |