ZNF93 zinc finger protein 93
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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88 |
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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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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 | HPF34 |
SYNONYM | HTF34 |
SYNONYM | TF34 |
SYNONYM | ZNF505 |
MIM | 603975 OMIM |
HGNC | HGNC:13169 HGNC |
Ensembl | ENSG00000184635 Ensembl |
AllianceGenome | HGNC:13169 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000592160.5 | hg38 | chr19 | 19,900,971 | 19,932,997 | 32,027 |
ENST00000343769.6 | hg38 | chr19 | 19,900,946 | 19,935,575 | 34,630 |
ENST00000591366.5 | hg38 | chr19 | 19,900,928 | 19,927,313 | 26,386 |
ENST00000591366.5 | hg19 | chr19 | 20,011,737 | 20,038,122 | 26,386 |
ENST00000343769.6 | hg19 | chr19 | 20,011,755 | 20,046,384 | 34,630 |
ENST00000592160.5 | hg19 | chr19 | 20,011,780 | 20,043,806 | 32,027 |
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