Search Thermo Fisher Scientific
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GTTGGGCCTGCTTGGTGGCTGCCAC[A/C]TTGCCCCGGGTCCCCGCCTTCCTGC
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 - 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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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 | 86 | Missense Mutation | AAG,AAT | K,N 11 | NP_067046.1 | |
XM_005249817.4 | 86 | Missense Mutation | AAG,AAT | K,N 11 | XP_005249874.1 | |
XM_011515463.2 | 86 | Missense Mutation | AAG,AAT | K,N 11 | XP_011513765.1 | |
XM_011515464.2 | 86 | Missense Mutation | AAG,AAT | K,N 11 | XP_011513766.1 | |
XM_011515465.2 | 86 | Missense Mutation | AAG,AAT | K,N 11 | XP_011513767.1 | |
XM_017012478.1 | 86 | Missense Mutation | AAG,AAT | K,N 11 | XP_016867967.1 | |
XM_017012479.1 | 86 | UTR 5 | XP_016867968.1 |