Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138079 MIM: 613993 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GCK 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
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CEPH (CEU) - Not Available | |||||||||
EAS
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African American
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YRI (Yoruba)
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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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GCK - glucokinase | ||||||
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There are no transcripts associated with this gene. |
MYL7 - myosin light chain 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021223.2 | 498 | Intron | NP_067046.1 | |||
XM_005249817.4 | 498 | Intron | XP_005249874.1 | |||
XM_011515463.2 | 498 | Intron | XP_011513765.1 | |||
XM_011515464.2 | 498 | Intron | XP_011513766.1 | |||
XM_011515465.2 | 498 | Missense Mutation | CCA,TCA | P,S 138 | XP_011513767.1 | |
XM_017012478.1 | 498 | Intron | XP_016867967.1 | |||
XM_017012479.1 | 498 | Intron | XP_016867968.1 |
Set Membership: |
HapMap Validated |