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- SNP ID:
- rs61563008
- Gene
-
FPR1FPR2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 51755424 - 51755424 on Build GRCh38
- Polymorphism:
- T/C, Transition substitution
- Context Sequence [VIC/FAM]:
GTTCAGACACATCATTTTGGGTTCC[T/C]GTTTCCTTTCAAACTCATCTGCAGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 136537
MIM: 136538
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Literature Links: |
FPR1 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
|
| FPR1 - formyl peptide receptor 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| FPR2 - formyl peptide receptor 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001005738.1 | Intron | NP_001005738.1 | ||||
| NM_001462.3 | Intron | NP_001453.1 | ||||
| XM_006723120.3 | Intron | XP_006723183.1 | ||||
| XM_017026542.1 | Intron | XP_016882031.1 | ||||
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