ZNF229 zinc finger protein 229
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 16 |
Uncertain significance | 0 | 114 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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130 |
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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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MIM | 620827 OMIM |
HGNC | HGNC:13022 HGNC |
Ensembl | ENSG00000278318 Ensembl |
AllianceGenome | HGNC:13022 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000614049.5 | hg38 | chr19 | 44,426,254 | 44,448,472 | 22,219 |
ENST00000613197.4 | hg38 | chr19 | 44,426,251 | 44,448,578 | 22,328 |
ENST00000613197.4 | hg19 | chr19 | 44,930,423 | 44,952,766 | 22,344 |
ENST00000614049.5 | hg19 | chr19 | 44,930,426 | 44,952,660 | 22,235 |
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