UBL7 ubiquitin like 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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32 |
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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
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 | BMSC-UbP |
SYNONYM | TCBA1 |
MIM | 609748 OMIM |
HGNC | HGNC:28221 HGNC |
Ensembl | ENSG00000138629 Ensembl |
AllianceGenome | HGNC:28221 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000361351.8 | hg38 | chr15 | 74,445,977 | 74,461,182 | 15,206 |
ENST00000567435.5 | hg38 | chr15 | 74,445,977 | 74,461,102 | 15,126 |
ENST00000564488.5 | hg38 | chr15 | 74,445,978 | 74,461,118 | 15,141 |
ENST00000395081.7 | hg38 | chr15 | 74,445,977 | 74,461,160 | 15,184 |
ENST00000565335.5 | hg38 | chr15 | 74,445,977 | 74,461,151 | 15,175 |
ENST00000567435.5 | hg19 | chr15 | 74,738,318 | 74,753,443 | 15,126 |
ENST00000565335.5 | hg19 | chr15 | 74,738,318 | 74,753,492 | 15,175 |
ENST00000395081.7 | hg19 | chr15 | 74,738,318 | 74,753,501 | 15,184 |
ENST00000361351.8 | hg19 | chr15 | 74,738,318 | 74,753,523 | 15,206 |
ENST00000564488.5 | hg19 | chr15 | 74,738,319 | 74,753,459 | 15,141 |
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