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 | |
---|---|
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0 |
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0 |
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50 |
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412 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | FMLP |
SYNONYM | FPR |
MIM | 136537 OMIM |
HGNC | HGNC:3826 HGNC |
Ensembl | ENSG00000171051 Ensembl |
AllianceGenome | HGNC:3826 |
Descrption | Source | Links |
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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 |
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