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AGAGACTACAGCCTCTCCCCCTACC[C/T]TGGAAGCTGCGATGCGCTGGTGAGG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610076 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDK20 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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CDK20 - cyclin dependent kinase 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039803.2 | 1152 | Missense Mutation | AAG,AGG | K,R 281 | NP_001034892.1 | |
NM_001170639.1 | 1152 | Missense Mutation | AAG,AGG | K,R 260 | NP_001164110.1 | |
NM_001170640.1 | 1152 | Missense Mutation | AGG,GGG | R,G 219 | NP_001164111.1 | |
NM_012119.4 | 1152 | Missense Mutation | AAG,AGG | K,R 260 | NP_036251.2 | |
NM_178432.3 | 1152 | Missense Mutation | AAG,AGG | K,R 273 | NP_848519.1 | |
XM_017014561.1 | 1152 | Missense Mutation | AAG,AGG | K,R 286 | XP_016870050.1 | |
XM_017014562.1 | 1152 | Missense Mutation | AAG,AGG | K,R 286 | XP_016870051.1 | |
XM_017014563.1 | 1152 | Missense Mutation | AGA,GGA | R,G 219 | XP_016870052.1 | |
XM_017014564.1 | 1152 | Missense Mutation | AAG,AGG | K,R 260 | XP_016870053.1 |
Set Membership: |
HapMap |