ZNF470 zinc finger protein 470
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 110 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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116 |
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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
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 | CZF-1 |
MIM | 620441 OMIM |
HGNC | HGNC:22220 HGNC |
Ensembl | ENSG00000197016 Ensembl |
AllianceGenome | HGNC:22220 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000601902.5 | hg38 | chr19 | 56,567,526 | 56,588,911 | 21,386 |
ENST00000330619.13 | hg38 | chr19 | 56,567,468 | 56,582,894 | 15,427 |
ENST00000391709.4 | hg38 | chr19 | 56,570,175 | 56,582,893 | 12,719 |
ENST00000330619.13 | hg19 | chr19 | 57,078,837 | 57,094,262 | 15,426 |
ENST00000601902.5 | hg19 | chr19 | 57,078,895 | 57,100,279 | 21,385 |
ENST00000391709.4 | hg19 | chr19 | 57,081,544 | 57,094,261 | 12,718 |
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