Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCCTGCGCAGGAACCCTCTAAGC[A/G]GAGTGCAGTGGGATAACAAACTTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 602990 MIM: 609842 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLK3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
CLK3 - CDC like kinase 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130028.1 | 1794 | Intron | NP_001123500.1 | |||
NM_003992.4 | 1794 | Intron | NP_003983.2 | |||
XM_005254151.3 | 1794 | Intron | XP_005254208.1 | |||
XM_011521205.2 | 1794 | Intron | XP_011519507.1 | |||
XM_011521206.2 | 1794 | Intron | XP_011519508.1 | |||
XM_011521209.2 | 1794 | Intron | XP_011519511.2 | |||
XM_017021905.1 | 1794 | Intron | XP_016877394.1 | |||
XM_017021906.1 | 1794 | Intron | XP_016877395.1 | |||
XM_017021907.1 | 1794 | Intron | XP_016877396.1 | |||
XM_017021908.1 | 1794 | Intron | XP_016877397.1 | |||
XM_017021909.1 | 1794 | Intron | XP_016877398.1 | |||
XM_017021910.1 | 1794 | Intron | XP_016877399.1 |
EDC3 - enhancer of mRNA decapping 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142443.1 | 1794 | Silent Mutation | TCC,TCT | S,S 507 | NP_001135915.1 | |
NM_001142444.1 | 1794 | Silent Mutation | TCC,TCT | S,S 507 | NP_001135916.1 | |
NM_025083.3 | 1794 | Silent Mutation | TCC,TCT | S,S 507 | NP_079359.2 | |
XM_011522092.2 | 1794 | Silent Mutation | TCC,TCT | S,S 324 | XP_011520394.1 |