ZNF182 zinc finger protein 182
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | HHZ150 |
SYNONYM | KOX14 |
SYNONYM | ZNF21 |
SYNONYM | Zfp182 |
MIM | 314993 OMIM |
HGNC | HGNC:13001 HGNC |
Ensembl | ENSG00000147118 Ensembl |
AllianceGenome | HGNC:13001 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000376943.8 | hg38 | chrX | 47,974,851 | 48,003,989 | 29,139 |
ENST00000396965.5 | hg38 | chrX | 47,974,852 | 48,003,978 | 29,127 |
ENST00000376943.8 | hg19 | chrX | 47,834,250 | 47,863,388 | 29,139 |
ENST00000396965.5 | hg19 | chrX | 47,834,251 | 47,863,377 | 29,127 |
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