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AGCAGGAGGCTGAGACGCCGCCAAC[C/T]TCGTCCTCCGGTTGCGGGGGCGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603461 MIM: 605530 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC16 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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CDC16 - cell division cycle 16 | ||||||
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There are no transcripts associated with this gene. |
MIR4502 - microRNA 4502 | ||||||
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There are no transcripts associated with this gene. |
UPF3A - UPF3 regulator of nonsense transcripts homolog A (yeast) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023011.3 | 197 | Silent Mutation | ACC,ACT | T,T 47 | NP_075387.1 | |
NM_080687.2 | 197 | Silent Mutation | ACC,ACT | T,T 47 | NP_542418.1 | |
XM_005266202.4 | 197 | Intron | XP_005266259.1 | |||
XM_006719991.3 | 197 | Intron | XP_006720054.1 | |||
XM_011534844.1 | 197 | Intron | XP_011533146.1 | |||
XM_011534845.2 | 197 | Intron | XP_011533147.1 | |||
XM_011534846.1 | 197 | Silent Mutation | ACC,ACT | T,T 47 | XP_011533148.1 | |
XM_011534847.2 | 197 | Intron | XP_011533149.1 | |||
XM_011534848.2 | 197 | Intron | XP_011533150.1 | |||
XM_017020709.1 | 197 | Intron | XP_016876198.1 | |||
XM_017020710.1 | 197 | Intron | XP_016876199.1 | |||
XM_017020711.1 | 197 | Intron | XP_016876200.1 | |||
XM_017020712.1 | 197 | Silent Mutation | ACC,ACT | T,T 47 | XP_016876201.1 |