ZNF180 zinc finger protein 180
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 80 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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84 |
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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 |
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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 | HHZ168 |
MIM | 606740 OMIM |
HGNC | HGNC:12970 HGNC |
Ensembl | ENSG00000167384 Ensembl |
AllianceGenome | HGNC:12970 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000391956.8 | hg38 | chr19 | 44,475,637 | 44,500,520 | 24,884 |
ENST00000221327.8 | hg38 | chr19 | 44,474,428 | 44,500,522 | 26,095 |
ENST00000587047.1 | hg38 | chr19 | 44,478,104 | 44,500,510 | 22,407 |
ENST00000592529.6 | hg38 | chr19 | 44,474,443 | 44,500,522 | 26,080 |
ENST00000221327.8 | hg19 | chr19 | 44,978,645 | 45,004,574 | 25,930 |
ENST00000592529.6 | hg19 | chr19 | 44,978,660 | 45,004,574 | 25,915 |
ENST00000391956.8 | hg19 | chr19 | 44,979,854 | 45,004,572 | 24,719 |
ENST00000587047.1 | hg19 | chr19 | 44,982,321 | 45,004,562 | 22,242 |
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