ZNF136 zinc finger protein 136
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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2 |
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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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 | pHZ-20 |
MIM | 604078 OMIM |
HGNC | HGNC:12920 HGNC |
Ensembl | ENSG00000196646 Ensembl |
AllianceGenome | HGNC:12920 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000343979.6 | hg38 | chr19 | 12,163,096 | 12,189,871 | 26,776 |
ENST00000652580.1 | hg38 | chr19 | 12,163,070 | 12,189,183 | 26,114 |
ENST00000652580.1 | hg19 | chr19 | 12,273,885 | 12,299,998 | 26,114 |
ENST00000343979.6 | hg19 | chr19 | 12,273,911 | 12,300,686 | 26,776 |
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