Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612977 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCUN1D4 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)
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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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DCUN1D4 - defective in cullin neddylation 1 domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040402.2 | Intron | NP_001035492.1 | ||||
NM_001287755.1 | Intron | NP_001274684.1 | ||||
NM_001287757.1 | Intron | NP_001274686.1 | ||||
NM_015115.3 | Intron | NP_055930.2 | ||||
XM_005265731.3 | Intron | XP_005265788.1 | ||||
XM_011534379.2 | Intron | XP_011532681.1 | ||||
XM_011534380.1 | Intron | XP_011532682.1 | ||||
XM_017007912.1 | Intron | XP_016863401.1 | ||||
XM_017007913.1 | Intron | XP_016863402.1 |