ZNF81 zinc finger protein 81
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 24 |
Likely benign | 0 | 20 |
Conflicting classifications of pathogenicity | 0 | 6 |
not provided | 6 | 0 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
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0 |
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0 |
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16 |
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80 |
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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
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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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 | HFZ20 |
SYNONYM | MRX45 |
SYNONYM | dJ54B20.6 |
MIM | 314998 OMIM |
HGNC | HGNC:13156 HGNC |
Ensembl | ENSG00000197779 Ensembl |
AllianceGenome | HGNC:13156 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000338637.13 | hg38 | chrX | 47,836,902 | 47,925,627 | 88,726 |
ENST00000376954.6 | hg38 | chrX | 47,836,902 | 47,925,627 | 88,726 |
ENST00000334937.8 | hg38 | chrX | 47,836,946 | 47,888,210 | 51,265 |
ENST00000338637.13 | hg19 | chrX | 47,696,301 | 47,785,026 | 88,726 |
ENST00000376954.6 | hg19 | chrX | 47,696,301 | 47,785,026 | 88,726 |
ENST00000334937.8 | hg19 | chrX | 47,696,345 | 47,747,609 | 51,265 |
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