CD84 CD84 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
risk factor | 0 | 2 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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
[No Data.]
Locus Zoom
Variants
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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 |
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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 | LY9B |
SYNONYM | SLAMF5 |
SYNONYM | hCD84 |
SYNONYM | mCD84 |
MIM | 604513 OMIM |
HGNC | HGNC:1704 HGNC |
Ensembl | ENSG00000066294 Ensembl |
AllianceGenome | HGNC:1704 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000534968.5 | hg38 | chr1 | 160,541,095 | 160,579,516 | 38,422 |
ENST00000368048.7 | hg38 | chr1 | 160,548,245 | 160,579,504 | 31,260 |
ENST00000368054.8 | hg38 | chr1 | 160,541,098 | 160,579,496 | 38,399 |
ENST00000368051.3 | hg38 | chr1 | 160,548,247 | 160,579,504 | 31,258 |
ENST00000311224.8 | hg38 | chr1 | 160,548,245 | 160,579,504 | 31,260 |
ENST00000534968.5 | hg19 | chr1 | 160,510,885 | 160,549,306 | 38,422 |
ENST00000368054.8 | hg19 | chr1 | 160,510,888 | 160,549,286 | 38,399 |
ENST00000311224.8 | hg19 | chr1 | 160,518,035 | 160,549,294 | 31,260 |
ENST00000368048.7 | hg19 | chr1 | 160,518,035 | 160,549,294 | 31,260 |
ENST00000368051.3 | hg19 | chr1 | 160,518,037 | 160,549,294 | 31,258 |
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