ZNF540 zinc finger protein 540
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 158 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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168 |
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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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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 | Nbla10512 |
MIM | 613903 OMIM |
HGNC | HGNC:25331 HGNC |
Ensembl | ENSG00000171817 Ensembl |
AllianceGenome | HGNC:25331 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000316433.9 | hg38 | chr19 | 37,594,876 | 37,614,179 | 19,304 |
ENST00000343599.5 | hg38 | chr19 | 37,595,253 | 37,614,095 | 18,843 |
ENST00000589117.5 | hg38 | chr19 | 37,594,830 | 37,613,387 | 18,558 |
ENST00000586792.5 | hg38 | chr19 | 37,594,973 | 37,611,872 | 16,900 |
ENST00000592533.5 | hg38 | chr19 | 37,551,406 | 37,614,095 | 62,690 |
ENST00000592533.5 | hg19 | chr19 | 38,042,308 | 38,104,996 | 62,689 |
ENST00000589117.5 | hg19 | chr19 | 38,085,731 | 38,104,288 | 18,558 |
ENST00000316433.9 | hg19 | chr19 | 38,085,777 | 38,105,080 | 19,304 |
ENST00000586792.5 | hg19 | chr19 | 38,085,874 | 38,102,773 | 16,900 |
ENST00000343599.5 | hg19 | chr19 | 38,086,154 | 38,104,996 | 18,843 |
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