FPR2 formyl peptide receptor 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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44 |
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0 |
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
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Target data | : |
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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 |
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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 | ALX |
SYNONYM | ALXR |
SYNONYM | FMLP-R-II |
SYNONYM | FMLPX |
SYNONYM | FPR2A |
SYNONYM | FPRH1 |
SYNONYM | FPRH2 |
SYNONYM | FPRL1 |
SYNONYM | HM63 |
SYNONYM | LXA4R |
MIM | 136538 OMIM |
HGNC | HGNC:3827 HGNC |
Ensembl | ENSG00000171049 Ensembl |
AllianceGenome | HGNC:3827 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000340023.7 | hg38 | chr19 | 51,761,180 | 51,770,531 | 9,352 |
ENST00000598776.1 | hg38 | chr19 | 51,762,760 | 51,770,507 | 7,748 |
ENST00000598953.1 | hg38 | chr19 | 51,761,212 | 51,770,013 | 8,802 |
ENST00000340023.7 | hg19 | chr19 | 52,264,433 | 52,273,784 | 9,352 |
ENST00000598953.1 | hg19 | chr19 | 52,264,465 | 52,273,266 | 8,802 |
ENST00000598776.1 | hg19 | chr19 | 52,266,013 | 52,273,760 | 7,748 |
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