ZNF208 zinc finger protein 208
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
not provided | 0 | 2 |
Uncertain significance | 0 | 188 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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200 |
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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
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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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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 | PMIDP |
SYNONYM | ZNF95 |
MIM | 603977 OMIM |
HGNC | HGNC:12999 HGNC |
Ensembl | ENSG00000160321 Ensembl |
AllianceGenome | HGNC:12999 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000397126.9 | hg38 | chr19 | 21,966,095 | 22,010,943 | 44,849 |
ENST00000597040.1 | hg38 | chr19 | 21,986,728 | 22,010,919 | 24,192 |
ENST00000599916.5 | hg38 | chr19 | 21,932,958 | 22,010,949 | 77,992 |
ENST00000601773.5 | hg38 | chr19 | 21,939,773 | 22,010,943 | 71,171 |
ENST00000599916.5 | hg19 | chr19 | 22,115,760 | 22,193,751 | 77,992 |
ENST00000601773.5 | hg19 | chr19 | 22,122,575 | 22,193,745 | 71,171 |
ENST00000397126.9 | hg19 | chr19 | 22,148,897 | 22,193,745 | 44,849 |
ENST00000597040.1 | hg19 | chr19 | 22,169,530 | 22,193,721 | 24,192 |
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