Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGATAAGAAGAATTTCGAAAACCC[A/G]GGTCCTTTTGCAACTGAATCTCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603440 | ||||||||||||||||||||
Literature Links: |
CDK17 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CDK17 - cyclin dependent kinase 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170464.2 | 2134 | Missense Mutation | CCG,CTG | P,L 501 | NP_001163935.1 | |
NM_002595.4 | 2134 | Missense Mutation | CCG,CTG | P,L 501 | NP_002586.2 | |
XM_017019405.1 | 2134 | Missense Mutation | CCG,CTG | P,L 501 | XP_016874894.1 | |
XM_017019406.1 | 2134 | Missense Mutation | CCG,CTG | P,L 501 | XP_016874895.1 | |
XM_017019407.1 | 2134 | Missense Mutation | CCG,CTG | P,L 480 | XP_016874896.1 |