ZNF264 zinc finger protein 264
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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100 |
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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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Target data | : |
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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MIM | 604668 OMIM |
HGNC | HGNC:13057 HGNC |
Ensembl | ENSG00000083844 Ensembl |
AllianceGenome | HGNC:13057 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000599653.1 | hg38 | chr19 | 57,191,537 | 57,194,169 | 2,633 |
ENST00000263095.10 | hg38 | chr19 | 57,191,500 | 57,222,846 | 31,347 |
ENST00000600531.5 | hg38 | chr19 | 57,191,501 | 57,194,969 | 3,469 |
ENST00000263095.10 | hg19 | chr19 | 57,702,868 | 57,734,214 | 31,347 |
ENST00000600531.5 | hg19 | chr19 | 57,702,869 | 57,706,337 | 3,469 |
ENST00000599653.1 | hg19 | chr19 | 57,702,905 | 57,705,537 | 2,633 |
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