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GGCCGCGCACCTGTCAGGTCGGGGG[A/G]CCTACGTGCGCCGCGACACGGCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602990 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLK3 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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CLK3 - CDC like kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130028.1 | 612 | Missense Mutation | ACC,GCC | T,A 51 | NP_001123500.1 | |
NM_003992.4 | 612 | Intron | NP_003983.2 | |||
XM_005254151.3 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_005254208.1 | |
XM_011521205.2 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_011519507.1 | |
XM_011521206.2 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_011519508.1 | |
XM_011521209.2 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_011519511.2 | |
XM_017021905.1 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_016877394.1 | |
XM_017021906.1 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_016877395.1 | |
XM_017021907.1 | 612 | Missense Mutation | ACC,GCC | T,A 51 | XP_016877396.1 | |
XM_017021908.1 | 612 | Intron | XP_016877397.1 | |||
XM_017021909.1 | 612 | Intron | XP_016877398.1 | |||
XM_017021910.1 | 612 | Intron | XP_016877399.1 |
LOC102723750 - uncharacterized LOC102723750 | ||||||
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There are no transcripts associated with this gene. |