WDR87 WD repeat domain 87
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 134 |
Likely benign | 0 | 144 |
Conflicting classifications of pathogenicity | 0 | 12 |
Uncertain significance | 0 | 370 |
Ranking
ClinVar | |
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0 |
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0 |
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116 |
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500 |
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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 | NYD-SP11 |
MIM | 620274 OMIM |
HGNC | HGNC:29934 HGNC |
Ensembl | ENSG00000171804 Ensembl |
AllianceGenome | HGNC:29934 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000303868.5 | hg38 | chr19 | 37,884,932 | 37,906,677 | 21,746 |
ENST00000447313.7 | hg38 | chr19 | 37,884,823 | 37,906,594 | 21,772 |
ENST00000447313.7 | hg19 | chr19 | 38,375,463 | 38,397,234 | 21,772 |
ENST00000303868.5 | hg19 | chr19 | 38,375,572 | 38,397,317 | 21,746 |
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