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TCCTCTGCAGGGAGTCTCTTGCTCT[C/G]GTTCTTGCTGTTCCTGCTCCTGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176805 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PTGS1 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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PTGS1 - prostaglandin-endoperoxide synthase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000962.3 | 329 | Missense Mutation | TCG,TGG | S,W 8 | NP_000953.2 | |
NM_001271164.1 | 329 | Missense Mutation | TCG,TGG | S,W 8 | NP_001258093.1 | |
NM_001271165.1 | 329 | Intron | NP_001258094.1 | |||
NM_001271166.1 | 329 | UTR 5 | NP_001258095.1 | |||
NM_001271367.1 | 329 | UTR 5 | NP_001258296.1 | |||
NM_001271368.1 | 329 | UTR 5 | NP_001258297.1 | |||
NM_080591.2 | 329 | Missense Mutation | TCG,TGG | S,W 8 | NP_542158.1 | |
XM_005252105.3 | 329 | UTR 5 | XP_005252162.1 | |||
XM_011518875.2 | 329 | UTR 5 | XP_011517177.1 | |||
XM_011518876.2 | 329 | UTR 5 | XP_011517178.1 | |||
XM_017014929.1 | 329 | UTR 5 | XP_016870418.1 |