USP15 ubiquitin specific peptidase 15
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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60 |
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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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Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 | UNPH-2 |
SYNONYM | UNPH4 |
MIM | 604731 OMIM |
HGNC | HGNC:12613 HGNC |
Ensembl | ENSG00000135655 Ensembl |
AllianceGenome | HGNC:12613 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000280377.10 | hg38 | chr12 | 62,260,404 | 62,416,389 | 155,986 |
ENST00000353364.7 | hg38 | chr12 | 62,260,338 | 62,416,389 | 156,052 |
ENST00000312635.10 | hg38 | chr12 | 62,260,397 | 62,336,690 | 76,294 |
ENST00000312635.10 | hg19 | chr12 | 62,654,178 | 62,730,471 | 76,294 |
ENST00000280377.10 | hg19 | chr12 | 62,654,185 | 62,810,169 | 155,985 |
ENST00000353364.7 | hg19 | chr12 | 62,654,119 | 62,810,169 | 156,051 |
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