WASHC3 WASH complex subunit 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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 | CCDC53 |
SYNONYM | CGI-116 |
MIM | 619925 OMIM |
HGNC | HGNC:24256 HGNC |
Ensembl | ENSG00000120860 Ensembl |
AllianceGenome | HGNC:24256 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000240079.11 | hg38 | chr12 | 102,012,840 | 102,061,991 | 49,152 |
ENST00000545679.5 | hg38 | chr12 | 102,012,942 | 102,062,079 | 49,138 |
ENST00000240079.11 | hg19 | chr12 | 102,406,618 | 102,455,769 | 49,152 |
ENST00000545679.5 | hg19 | chr12 | 102,406,720 | 102,455,857 | 49,138 |
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