UBL5 ubiquitin like 5
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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2 |
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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
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | HUB1 |
| MIM | 606849 OMIM |
| HGNC | HGNC:13736 HGNC |
| Ensembl | ENSG00000198258 Ensembl |
| AllianceGenome | HGNC:13736 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000593087.1 | hg38 | chr19 | 9,827,915 | 9,830,113 | 2,199 |
| ENST00000358666.7 | hg38 | chr19 | 9,827,892 | 9,830,115 | 2,224 |
| ENST00000586895.6 | hg38 | chr19 | 9,827,918 | 9,830,115 | 2,198 |
| ENST00000590068.1 | hg38 | chr19 | 9,827,894 | 9,830,115 | 2,222 |
| ENST00000358666.7 | hg19 | chr19 | 9,938,568 | 9,940,791 | 2,224 |
| ENST00000590068.1 | hg19 | chr19 | 9,938,570 | 9,940,791 | 2,222 |
| ENST00000593087.1 | hg19 | chr19 | 9,938,591 | 9,940,789 | 2,199 |
| ENST00000586895.6 | hg19 | chr19 | 9,938,594 | 9,940,791 | 2,198 |
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