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CAGCAGCCCCTATTCTCGGCGGCTG[C/G]CGCGCTCCCCGAGCCCCTACAGTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603309 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDK13 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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CDK13 - cyclin dependent kinase 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003718.4 | 2207 | Missense Mutation | CCG,GCG | P,A 356 | NP_003709.3 | |
NM_031267.3 | 2207 | Missense Mutation | CCG,GCG | P,A 356 | NP_112557.2 | |
XM_011515597.2 | 2207 | Missense Mutation | CCG,GCG | P,A 356 | XP_011513899.1 | |
XM_017012750.1 | 2207 | Missense Mutation | CCG,GCG | P,A 356 | XP_016868239.1 | |
XM_017012751.1 | 2207 | Missense Mutation | CCG,GCG | P,A 356 | XP_016868240.1 |