ZNF568 zinc finger protein 568
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 72 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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76 |
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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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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | ZFP568 |
MIM | 617566 OMIM |
HGNC | HGNC:25392 HGNC |
Ensembl | ENSG00000198453 Ensembl |
AllianceGenome | HGNC:25392 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000444991.6 | hg38 | chr19 | 36,916,325 | 37,005,037 | 88,713 |
ENST00000415168.5 | hg38 | chr19 | 36,916,343 | 36,952,743 | 36,401 |
ENST00000427117.6 | hg38 | chr19 | 36,916,316 | 36,981,837 | 65,522 |
ENST00000586353.6 | hg38 | chr19 | 36,973,213 | 36,981,857 | 8,645 |
ENST00000455427.7 | hg38 | chr19 | 36,916,341 | 36,998,300 | 81,960 |
ENST00000587857.6 | hg38 | chr19 | 36,916,332 | 36,951,704 | 35,373 |
ENST00000587130.6 | hg38 | chr19 | 36,916,341 | 36,951,640 | 35,300 |
ENST00000706172.1 | hg38 | chr19 | 36,973,422 | 37,003,369 | 29,948 |
ENST00000706173.1 | hg38 | chr19 | 36,973,538 | 36,998,339 | 24,802 |
ENST00000706170.1 | hg38 | chr19 | 36,916,350 | 36,951,704 | 35,355 |
ENST00000706169.1 | hg38 | chr19 | 36,916,341 | 37,002,593 | 86,253 |
ENST00000706166.1 | hg38 | chr19 | 36,916,326 | 36,981,837 | 65,512 |
ENST00000706167.1 | hg38 | chr19 | 36,916,332 | 36,952,734 | 36,403 |
ENST00000333987.12 | hg38 | chr19 | 36,916,332 | 36,952,734 | 36,403 |
ENST00000427117.6 | hg19 | chr19 | 37,407,218 | 37,472,739 | 65,522 |
ENST00000444991.6 | hg19 | chr19 | 37,407,227 | 37,495,939 | 88,713 |
ENST00000415168.5 | hg19 | chr19 | 37,407,245 | 37,443,645 | 36,401 |
ENST00000706166.1 | hg19 | chr19 | 37,407,228 | 37,472,739 | 65,512 |
ENST00000333987.12 | hg19 | chr19 | 37,407,234 | 37,443,636 | 36,403 |
ENST00000586353.6 | hg19 | chr19 | 37,464,115 | 37,472,759 | 8,645 |
ENST00000587857.6 | hg19 | chr19 | 37,407,234 | 37,442,606 | 35,373 |
ENST00000455427.7 | hg19 | chr19 | 37,407,243 | 37,489,202 | 81,960 |
ENST00000587130.6 | hg19 | chr19 | 37,407,243 | 37,442,542 | 35,300 |
ENST00000706167.1 | hg19 | chr19 | 37,407,234 | 37,443,636 | 36,403 |
ENST00000706169.1 | hg19 | chr19 | 37,407,243 | 37,493,495 | 86,253 |
ENST00000706170.1 | hg19 | chr19 | 37,407,252 | 37,442,606 | 35,355 |
ENST00000706172.1 | hg19 | chr19 | 37,464,324 | 37,494,271 | 29,948 |
ENST00000706173.1 | hg19 | chr19 | 37,464,440 | 37,489,241 | 24,802 |
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