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GCGTCTACATTCACGGCGGTCACTC[C/T]GTTTCTGTCTCCTTTTGTTTGGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602743 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRKAG2 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
PRKAG2 - protein kinase AMP-activated non-catalytic subunit gamma 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040633.1 | 2080 | Silent Mutation | ACA,ACG | T,T 524 | NP_001035723.1 | |
NM_001304527.1 | 2080 | Silent Mutation | ACA,ACG | T,T 443 | NP_001291456.1 | |
NM_001304531.1 | 2080 | Silent Mutation | ACA,ACG | T,T 327 | NP_001291460.1 | |
NM_016203.3 | 2080 | Silent Mutation | ACA,ACG | T,T 568 | NP_057287.2 | |
NM_024429.1 | 2080 | Silent Mutation | ACA,ACG | T,T 327 | NP_077747.1 | |
XM_005250002.3 | 2080 | UTR 3 | XP_005250059.1 | |||
XM_005250004.3 | 2080 | UTR 3 | XP_005250061.1 | |||
XM_005250006.4 | 2080 | UTR 3 | XP_005250063.1 | |||
XM_006716021.2 | 2080 | UTR 3 | XP_006716084.1 | |||
XM_011516282.1 | 2080 | UTR 3 | XP_011514584.1 | |||
XM_011516283.1 | 2080 | Silent Mutation | ACA,ACG | T,T 564 | XP_011514585.1 | |
XM_011516284.1 | 2080 | Silent Mutation | ACA,ACG | T,T 563 | XP_011514586.1 | |
XM_011516285.1 | 2080 | UTR 3 | XP_011514587.1 | |||
XM_011516286.1 | 2080 | UTR 3 | XP_011514588.1 | |||
XM_011516287.1 | 2080 | UTR 3 | XP_011514589.1 | |||
XM_017012268.1 | 2080 | UTR 3 | XP_016867757.1 | |||
XM_017012269.1 | 2080 | Silent Mutation | ACA,ACG | T,T 567 | XP_016867758.1 | |
XM_017012270.1 | 2080 | Silent Mutation | ACA,ACG | T,T 524 | XP_016867759.1 | |
XM_017012271.1 | 2080 | Silent Mutation | ACA,ACG | T,T 523 | XP_016867760.1 | |
XM_017012272.1 | 2080 | Silent Mutation | ACA,ACG | T,T 523 | XP_016867761.1 | |
XM_017012273.1 | 2080 | Silent Mutation | ACA,ACG | T,T 444 | XP_016867762.1 | |
XM_017012274.1 | 2080 | UTR 3 | XP_016867763.1 | |||
XM_017012275.1 | 2080 | UTR 3 | XP_016867764.1 | |||
XM_017012276.1 | 2080 | Silent Mutation | ACA,ACG | T,T 326 | XP_016867765.1 | |
XM_017012277.1 | 2080 | Silent Mutation | ACA,ACG | T,T 319 | XP_016867766.1 | |
XM_017012278.1 | 2080 | Silent Mutation | ACA,ACG | T,T 307 | XP_016867767.1 | |
XM_017012279.1 | 2080 | Silent Mutation | ACA,ACG | T,T 307 | XP_016867768.1 | |
XM_017012280.1 | 2080 | Silent Mutation | ACA,ACG | T,T 307 | XP_016867769.1 | |
XM_017012281.1 | 2080 | Silent Mutation | ACA,ACG | T,T 307 | XP_016867770.1 | |
XM_017012282.1 | 2080 | Silent Mutation | ACA,ACG | T,T 307 | XP_016867771.1 |