FCAR Fc alpha receptor
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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
[No Data.]
Locus Zoom
Variants
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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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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 | CD89 |
SYNONYM | CTB-61M7.2 |
SYNONYM | FcalphaR |
SYNONYM | FcalphaRI |
MIM | 147045 OMIM |
HGNC | HGNC:3608 HGNC |
Ensembl | ENSG00000186431 Ensembl |
AllianceGenome | HGNC:3608 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000391724.3 | hg38 | chr19 | 54,874,290 | 54,889,863 | 15,574 |
ENST00000391723.7 | hg38 | chr19 | 54,874,290 | 54,889,863 | 15,574 |
ENST00000391726.7 | hg38 | chr19 | 54,874,248 | 54,889,890 | 15,643 |
ENST00000391725.7 | hg38 | chr19 | 54,874,285 | 54,889,890 | 15,606 |
ENST00000359272.8 | hg38 | chr19 | 54,874,290 | 54,889,863 | 15,574 |
ENST00000345937.8 | hg38 | chr19 | 54,874,285 | 54,889,890 | 15,606 |
ENST00000353758.8 | hg38 | chr19 | 54,874,290 | 54,889,863 | 15,574 |
ENST00000355524.8 | hg38 | chr19 | 54,874,235 | 54,891,420 | 17,186 |
ENST00000469767.5 | hg38 | chr19 | 54,874,280 | 54,889,067 | 14,788 |
ENST00000355524.8 | hg19 | chr19 | 55,385,691 | 55,402,786 | 17,096 |
ENST00000391726.7 | hg19 | chr19 | 55,385,704 | 55,401,256 | 15,553 |
ENST00000469767.5 | hg19 | chr19 | 55,385,736 | 55,400,434 | 14,699 |
ENST00000345937.8 | hg19 | chr19 | 55,385,741 | 55,401,256 | 15,516 |
ENST00000391725.7 | hg19 | chr19 | 55,385,741 | 55,401,256 | 15,516 |
ENST00000353758.8 | hg19 | chr19 | 55,385,746 | 55,401,229 | 15,484 |
ENST00000359272.8 | hg19 | chr19 | 55,385,746 | 55,401,229 | 15,484 |
ENST00000391723.7 | hg19 | chr19 | 55,385,746 | 55,401,229 | 15,484 |
ENST00000391724.3 | hg19 | chr19 | 55,385,746 | 55,401,229 | 15,484 |
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