Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613131 MIM: 613132 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC20B 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CDC20B - cell division cycle 20B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145734.2 | 358 | Intron | NP_001139206.2 | |||
NM_001170402.1 | 358 | Intron | NP_001163873.1 | |||
NM_152623.2 | 358 | Intron | NP_689836.2 | |||
XM_011543218.2 | 358 | Intron | XP_011541520.1 |
GPX8 - glutathione peroxidase 8 (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008397.3 | 358 | Missense Mutation | AAG,AGG | K,R 182 | NP_001008398.2 | |
NM_001306197.1 | 358 | Missense Mutation | AAG,AGG | K,R 131 | NP_001293126.1 | |
NM_001306198.1 | 358 | UTR 3 | NP_001293127.1 | |||
NM_001306201.1 | 358 | Missense Mutation | AAG,AGG | K,R 89 | NP_001293130.1 | |
XM_006714631.2 | 358 | Missense Mutation | AAG,AGG | K,R 183 | XP_006714694.1 |
MIR449A - microRNA 449a | ||||||
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There are no transcripts associated with this gene. |
MIR449B - microRNA 449b | ||||||
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There are no transcripts associated with this gene. |
MIR449C - microRNA 449c | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |