FCRL1 Fc receptor like 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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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 |
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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 | CD307a |
SYNONYM | FCRH1 |
SYNONYM | IFGP1 |
SYNONYM | IRTA5 |
MIM | 606508 OMIM |
HGNC | HGNC:18509 HGNC |
Ensembl | ENSG00000163534 Ensembl |
AllianceGenome | HGNC:18509 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368176.8 | hg38 | chr1 | 157,794,403 | 157,820,120 | 25,718 |
ENST00000358292.7 | hg38 | chr1 | 157,794,536 | 157,820,089 | 25,554 |
ENST00000491942.1 | hg38 | chr1 | 157,795,855 | 157,820,060 | 24,206 |
ENST00000368176.8 | hg19 | chr1 | 157,764,193 | 157,789,910 | 25,718 |
ENST00000358292.7 | hg19 | chr1 | 157,764,326 | 157,789,879 | 25,554 |
ENST00000491942.1 | hg19 | chr1 | 157,765,645 | 157,789,850 | 24,206 |
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