UBN1 ubinuclein 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 18 |
Likely benign | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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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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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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 | VT |
SYNONYM | VT4 |
MIM | 609771 OMIM |
HGNC | HGNC:12506 HGNC |
Ensembl | ENSG00000118900 Ensembl |
AllianceGenome | HGNC:12506 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000590769.5 | hg38 | chr16 | 4,848,380 | 4,880,294 | 31,915 |
ENST00000396658.8 | hg38 | chr16 | 4,852,215 | 4,882,360 | 30,146 |
ENST00000262376.11 | hg38 | chr16 | 4,847,481 | 4,882,401 | 34,921 |
ENST00000262376.11 | hg19 | chr16 | 4,897,482 | 4,932,402 | 34,921 |
ENST00000590769.5 | hg19 | chr16 | 4,898,381 | 4,930,295 | 31,915 |
ENST00000396658.8 | hg19 | chr16 | 4,902,216 | 4,932,361 | 30,146 |
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