ZFP57 ZFP57 zinc finger protein
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 16 |
Likely pathogenic | 0 | 8 |
Benign | 0 | 50 |
Likely benign | 0 | 32 |
Conflicting classifications of pathogenicity | 0 | 20 |
not provided | 2 | 0 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
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0 |
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0 |
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36 |
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136 |
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18 |
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
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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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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 | C6orf40 |
SYNONYM | TNDM1 |
SYNONYM | ZNF698 |
SYNONYM | bA145L22 |
SYNONYM | bA145L22.2 |
MIM | 612192 OMIM |
HGNC | HGNC:18791 HGNC |
Ensembl | ENSG00000204644 Ensembl |
AllianceGenome | HGNC:18791 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000376883.2 | hg38 | chr6 | 29,672,483 | 29,681,152 | 8,670 |
ENST00000488757.6 | hg38 | chr6 | 29,672,483 | 29,681,155 | 8,673 |
ENST00000376883.2 | hg19 | chr6 | 29,640,260 | 29,648,929 | 8,670 |
ENST00000488757.6 | hg19 | chr6 | 29,640,260 | 29,648,932 | 8,673 |
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