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ATTGAAGTCGACACTAAGCCAATTA[A/G]GCTATAAATCAATACAAATATCACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607061 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PTGES3 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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PTGES3 - prostaglandin E synthase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282601.1 | 696 | Missense Mutation | CCT,CTT | P,L 96 | NP_001269530.1 | |
NM_001282602.1 | 696 | Intron | NP_001269531.1 | |||
NM_001282603.1 | 696 | Missense Mutation | CCT,CTT | P,L 63 | NP_001269532.1 | |
NM_001282604.1 | 696 | Missense Mutation | CCT,CTT | P,L 100 | NP_001269533.1 | |
NM_001282605.1 | 696 | Intron | NP_001269534.1 | |||
NM_006601.6 | 696 | Missense Mutation | CCT,CTT | P,L 96 | NP_006592.3 | |
XM_005268576.4 | 696 | Missense Mutation | CCT,CTT | P,L 100 | XP_005268633.1 | |
XM_006719199.2 | 696 | Intron | XP_006719262.1 | |||
XM_011537773.2 | 696 | Intron | XP_011536075.1 | |||
XM_011537774.2 | 696 | Missense Mutation | CCT,CTT | P,L 100 | XP_011536076.1 | |
XM_017018716.1 | 696 | Missense Mutation | CCT,CTT | P,L 100 | XP_016874205.1 |