Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 602989 MIM: 606913 | |||||||||||||||||||||||
Literature Links: |
CLK2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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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 |
CLK2 - CDC like kinase 2 | ||||||
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There are no transcripts associated with this gene. |
FAM189B - family with sequence similarity 189 member B | ||||||
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There are no transcripts associated with this gene. |
SCAMP3 - secretory carrier membrane protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005698.3 | 860 | Missense Mutation | GCT,GTT | A,V 235 | NP_005689.2 | |
NM_052837.2 | 860 | Missense Mutation | GCT,GTT | A,V 209 | NP_443069.1 | |
XM_006711105.3 | 860 | Missense Mutation | GCT,GTT | A,V 221 | XP_006711168.1 | |
XM_006711106.3 | 860 | Missense Mutation | GCT,GTT | A,V 168 | XP_006711169.1 | |
XM_016999991.1 | 860 | Intron | XP_016855480.1 |
Set Membership: |
HapMap |