Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCGCCAGGTCCATGGGTGTCAGGG[A/C]GAACATCTGCTCCACCTGCAGGGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 138079 MIM: 613993 | ||||||||||||||||||||
Literature Links: |
GCK PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
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 |
GCK - glucokinase | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
MYL7 - myosin light chain 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021223.2 | 535 | Missense Mutation | NP_067046.1 | |||
XM_005249817.4 | 535 | Silent Mutation | XP_005249874.1 | |||
XM_011515463.2 | 535 | Missense Mutation | XP_011513765.1 | |||
XM_011515464.2 | 535 | Missense Mutation | XP_011513766.1 | |||
XM_011515465.2 | 535 | UTR 3 | XP_011513767.1 | |||
XM_017012478.1 | 535 | Silent Mutation | XP_016867967.1 | |||
XM_017012479.1 | 535 | Missense Mutation | XP_016867968.1 |