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- SNP ID:
- rs199542450
- Gene
-
PTGER4 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.5: 40681682 - 40681682 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TCGCTGGGCACCGAGCAGCACCACG[A/C]GGCCGCGGCCGCCTCGGTTGCCTCC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601586
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Literature Links: |
PTGER4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
| PTGER4 - prostaglandin E receptor 4 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000958.2 | 1281 | Missense Mutation | GAG,GCG | E,A 230 | NP_000949.1 | |
| XM_017009656.1 | 1281 | Missense Mutation | GAG,GCG | E,A 230 | XP_016865145.1 | |
| XM_017009657.1 | 1281 | Missense Mutation | GAG,GCG | E,A 230 | XP_016865146.1 | |
| XM_017009658.1 | 1281 | Missense Mutation | GAG,GCG | E,A 230 | XP_016865147.1 | |
| XM_017009659.1 | 1281 | Missense Mutation | GAG,GCG | E,A 230 | XP_016865148.1 | |
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