FPR1 formyl peptide receptor 1
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 38 |
| Likely benign | 0 | 150 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| not provided | 8 | 0 |
| Uncertain significance | 0 | 282 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
50 |
![]() |
412 |
![]() |
2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | FMLP |
| SYNONYM | FPR |
| MIM | 136537 OMIM |
| HGNC | HGNC:3826 HGNC |
| Ensembl | ENSG00000171051 Ensembl |
| AllianceGenome | HGNC:3826 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000595042.5 | hg38 | chr19 | 51,745,172 | 51,751,893 | 6,722 |
| ENST00000594900.2 | hg38 | chr19 | 51,745,773 | 51,804,115 | 58,343 |
| ENST00000600815.2 | hg38 | chr19 | 51,745,773 | 51,750,811 | 5,039 |
| ENST00000304748.5 | hg38 | chr19 | 51,745,773 | 51,751,878 | 6,106 |
| ENST00000595042.5 | hg19 | chr19 | 52,248,425 | 52,255,146 | 6,722 |
| ENST00000600815.2 | hg19 | chr19 | 52,249,026 | 52,254,064 | 5,039 |
| ENST00000304748.5 | hg19 | chr19 | 52,249,026 | 52,255,131 | 6,106 |
| ENST00000594900.2 | hg19 | chr19 | 52,249,026 | 52,307,368 | 58,343 |
Genome browser




