USP32 ubiquitin specific peptidase 32
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 132 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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134 |
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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
Search Word
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 | NY-REN-60 |
SYNONYM | USP10 |
MIM | 607740 OMIM |
HGNC | HGNC:19143 HGNC |
Ensembl | ENSG00000170832 Ensembl |
AllianceGenome | HGNC:19143 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000300896.9 | hg38 | chr17 | 60,177,327 | 60,392,133 | 214,807 |
ENST00000393003.7 | hg38 | chr17 | 60,249,058 | 60,391,975 | 142,918 |
ENST00000592339.5 | hg38 | chr17 | 60,179,105 | 60,256,700 | 77,596 |
ENST00000300896.9 | hg19 | chr17 | 58,254,688 | 58,469,494 | 214,807 |
ENST00000592339.5 | hg19 | chr17 | 58,256,466 | 58,334,061 | 77,596 |
ENST00000393003.7 | hg19 | chr17 | 58,326,419 | 58,469,336 | 142,918 |
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