IGSF8 immunoglobulin superfamily member 8
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 102 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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104 |
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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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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 | CD316 |
SYNONYM | CD81P3 |
SYNONYM | EWI-2 |
SYNONYM | EWI2 |
SYNONYM | KCT-4 |
SYNONYM | LIR-D1 |
SYNONYM | PGRL |
MIM | 606644 OMIM |
HGNC | HGNC:17813 HGNC |
Ensembl | ENSG00000162729 Ensembl |
AllianceGenome | HGNC:17813 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000314485.12 | hg38 | chr1 | 160,091,343 | 160,098,619 | 7,277 |
ENST00000614243.4 | hg38 | chr1 | 160,091,350 | 160,098,828 | 7,479 |
ENST00000368086.5 | hg38 | chr1 | 160,091,340 | 160,098,689 | 7,350 |
ENST00000368086.5 | hg19 | chr1 | 160,061,130 | 160,068,479 | 7,350 |
ENST00000314485.12 | hg19 | chr1 | 160,061,133 | 160,068,409 | 7,277 |
ENST00000614243.4 | hg19 | chr1 | 160,061,140 | 160,068,618 | 7,479 |
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