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ATAGGTGCTAGGTGTACCCTCTGCA[C/T]AGCAGAACCGATTTCTTTTTTCAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612325 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ICK 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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ICK - intestinal cell (MAK-like) kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014920.3 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | NP_055735.1 | |
NM_016513.4 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | NP_057597.2 | |
XM_011514419.1 | 2882 | Missense Mutation | ATG,GTG | M,V 575 | XP_011512721.1 | |
XM_011514420.2 | 2882 | Missense Mutation | ATG,GTG | M,V 575 | XP_011512722.1 | |
XM_011514421.1 | 2882 | Missense Mutation | ATG,GTG | M,V 575 | XP_011512723.1 | |
XM_017010485.1 | 2882 | Missense Mutation | ATG,GTG | M,V 575 | XP_016865974.1 | |
XM_017010486.1 | 2882 | Missense Mutation | ATG,GTG | M,V 575 | XP_016865975.1 | |
XM_017010487.1 | 2882 | Missense Mutation | ATG,GTG | M,V 575 | XP_016865976.1 | |
XM_017010488.1 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | XP_016865977.1 | |
XM_017010489.1 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | XP_016865978.1 | |
XM_017010490.1 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | XP_016865979.1 | |
XM_017010491.1 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | XP_016865980.1 | |
XM_017010492.1 | 2882 | Missense Mutation | ATG,GTG | M,V 568 | XP_016865981.1 |