VEZF1 vascular endothelial zinc finger 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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2 |
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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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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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 | CMD1OO |
SYNONYM | DB1 |
SYNONYM | ZNF161 |
MIM | 606747 OMIM |
HGNC | HGNC:12949 HGNC |
Ensembl | ENSG00000136451 Ensembl |
AllianceGenome | HGNC:12949 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000584396.5 | hg38 | chr17 | 57,973,759 | 57,985,348 | 11,590 |
ENST00000581208.2 | hg38 | chr17 | 57,971,552 | 57,988,254 | 16,703 |
ENST00000581208.2 | hg19 | chr17 | 56,048,913 | 56,065,615 | 16,703 |
ENST00000584396.5 | hg19 | chr17 | 56,051,120 | 56,062,709 | 11,590 |
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