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AAGACACTATATTCTTTGTGTGTGA[C/T]ACCCATAGGCCAGTCAATGTCGTCA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603465 MIM: 601754 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC45 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)
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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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CDC45 - cell division cycle 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001178010.2 | 440 | Silent Mutation | GAC,GAT | D,D 99 | NP_001171481.1 | |
NM_001178011.2 | 440 | Intron | NP_001171482.1 | |||
NM_003504.4 | 440 | Silent Mutation | GAC,GAT | D,D 99 | NP_003495.1 | |
XM_005261285.2 | 440 | Silent Mutation | GAC,GAT | D,D 99 | XP_005261342.1 | |
XM_005261286.3 | 440 | Silent Mutation | GAC,GAT | D,D 99 | XP_005261343.1 | |
XM_011530415.1 | 440 | Silent Mutation | GAC,GAT | D,D 99 | XP_011528717.1 | |
XM_011530416.1 | 440 | Silent Mutation | GAC,GAT | D,D 87 | XP_011528718.1 | |
XM_011530417.2 | 440 | Intron | XP_011528719.1 | |||
XM_011530418.2 | 440 | Intron | XP_011528720.1 | |||
XM_017028966.1 | 440 | Intron | XP_016884455.1 | |||
XM_017028967.1 | 440 | Intron | XP_016884456.1 |
UFD1L - ubiquitin fusion degradation 1 like (yeast) | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |