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AATAGTTATGTCCTTAATGTGTACA[G/T]CATTAAGAGGTCGGTATGTCTTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601951 MIM: 615811 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLK1 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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CLK1 - CDC like kinase 1 | ||||||
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There are no transcripts associated with this gene. |
PPIL3 - peptidylprolyl isomerase like 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032472.3 | 700 | Missense Mutation | GAT,GCT | D,A 150 | NP_115861.1 | |
NM_130906.2 | 700 | Missense Mutation | GAT,GCT | D,A 146 | NP_570981.1 | |
XM_005246651.3 | 700 | Missense Mutation | GAT,GCT | D,A 150 | XP_005246708.1 | |
XM_005246652.4 | 700 | Missense Mutation | GAT,GCT | D,A 146 | XP_005246709.1 | |
XM_011511358.2 | 700 | Missense Mutation | GAT,GCT | D,A 146 | XP_011509660.1 | |
XM_017004352.1 | 700 | Missense Mutation | GAT,GCT | D,A 150 | XP_016859841.1 | |
XM_017004353.1 | 700 | Missense Mutation | GAT,GCT | D,A 150 | XP_016859842.1 | |
XM_017004354.1 | 700 | Intron | XP_016859843.1 | |||
XM_017004355.1 | 700 | Intron | XP_016859844.1 | |||
XM_017004356.1 | 700 | Intron | XP_016859845.1 | |||
XM_017004357.1 | 700 | Missense Mutation | GAT,GCT | D,A 97 | XP_016859846.1 | |
XM_017004358.1 | 700 | Missense Mutation | GAT,GCT | D,A 97 | XP_016859847.1 | |
XM_017004359.1 | 700 | Missense Mutation | GAT,GCT | D,A 97 | XP_016859848.1 | |
XM_017004360.1 | 700 | Missense Mutation | GAT,GCT | D,A 97 | XP_016859849.1 |