ZNF91 zinc finger protein 91
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 124 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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136 |
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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
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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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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 | HPF7 |
SYNONYM | HTF10 |
MIM | 603971 OMIM |
HGNC | HGNC:13166 HGNC |
Ensembl | ENSG00000167232 Ensembl |
AllianceGenome | HGNC:13166 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000397082.2 | hg38 | chr19 | 23,359,403 | 23,395,446 | 36,044 |
ENST00000599743.5 | hg38 | chr19 | 23,338,749 | 23,395,457 | 56,709 |
ENST00000300619.12 | hg38 | chr19 | 23,357,696 | 23,395,471 | 37,776 |
ENST00000599743.5 | hg19 | chr19 | 23,521,551 | 23,578,259 | 56,709 |
ENST00000300619.12 | hg19 | chr19 | 23,540,498 | 23,578,273 | 37,776 |
ENST00000397082.2 | hg19 | chr19 | 23,542,205 | 23,578,248 | 36,044 |
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