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CGGACGGGTCCTTTGGTACATGCAG[C/T]CCGAGGTGAGTCCCCTCCTTTCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 311550 MIM: 314370 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDK16 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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CDK16 - cyclin dependent kinase 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170460.1 | 779 | Intron | NP_001163931.1 | |||
NM_006201.4 | 779 | Intron | NP_006192.1 | |||
NM_033018.3 | 779 | Missense Mutation | CCC,TCC | P,S 3 | NP_148978.2 | |
XM_011543920.2 | 779 | Intron | XP_011542222.1 | |||
XM_011543921.1 | 779 | Silent Mutation | AGC,AGT | S,S 16 | XP_011542223.1 | |
XM_011543922.1 | 779 | Silent Mutation | AGC,AGT | S,S 16 | XP_011542224.1 | |
XM_011543923.1 | 779 | Missense Mutation | CCC,TCC | P,S 3 | XP_011542225.1 | |
XM_011543924.1 | 779 | Intron | XP_011542226.1 | |||
XM_011543925.2 | 779 | Intron | XP_011542227.1 | |||
XM_011543926.1 | 779 | Intron | XP_011542228.1 | |||
XM_011543927.2 | 779 | Intron | XP_011542229.1 | |||
XM_011543928.1 | 779 | UTR 5 | XP_011542230.1 | |||
XM_017029569.1 | 779 | Silent Mutation | AGC,AGT | S,S 16 | XP_016885058.1 | |
XM_017029570.1 | 779 | Intron | XP_016885059.1 | |||
XM_017029571.1 | 779 | Intron | XP_016885060.1 | |||
XM_017029572.1 | 779 | Intron | XP_016885061.1 | |||
XM_017029573.1 | 779 | UTR 5 | XP_016885062.1 |
UBA1 - ubiquitin like modifier activating enzyme 1 | ||||||
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There are no transcripts associated with this gene. |