FCRL4 Fc receptor like 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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56 |
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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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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 | CD307d |
SYNONYM | FCRH4 |
SYNONYM | IGFP2 |
SYNONYM | IRTA1 |
MIM | 605876 OMIM |
HGNC | HGNC:18507 HGNC |
Ensembl | ENSG00000163518 Ensembl |
AllianceGenome | HGNC:18507 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000271532.2 | hg38 | chr1 | 157,573,747 | 157,598,085 | 24,339 |
ENST00000271532.2 | hg19 | chr1 | 157,543,537 | 157,567,875 | 24,339 |
Key | Value |
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strand | - |
start | 157,543,538 |
Gene Symbol | FCRL4 |
Entrez GeneId | 83,417 |
Chr Band | 1q21 |
end | 157,567,869 |
chr | chr1 |
Name | Fc receptor-like 4 |
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