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CAAAGTAGCCCCAGCCTTCATCGCG[C/T]CTCATCTGCTCTGAAAATCCACTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616522 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCUN1D5 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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DCUN1D5 - defective in cullin neddylation 1 domain containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318739.1 | 11594 | UTR 3 | NP_001305668.1 | |||
NM_001318740.1 | 11594 | UTR 3 | NP_001305669.1 | |||
NM_001318741.1 | 11594 | UTR 3 | NP_001305670.1 | |||
NM_032299.3 | 11594 | UTR 3 | NP_115675.1 | |||
XM_017018404.1 | 11594 | Intron | XP_016873893.1 |