ZNF75D zinc finger protein 75D
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 8 |
not provided | 6 | 0 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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54 |
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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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Target data | : |
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 | D8C6 |
SYNONYM | ZKSCAN24 |
SYNONYM | ZNF75 |
SYNONYM | ZNF82 |
SYNONYM | ZSCAN28 |
MIM | 314997 OMIM |
HGNC | HGNC:13145 HGNC |
Ensembl | ENSG00000186376 Ensembl |
AllianceGenome | HGNC:13145 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000370764.1 | hg38 | chrX | 135,285,792 | 135,296,033 | 10,242 |
ENST00000370766.8 | hg38 | chrX | 135,285,791 | 135,344,109 | 58,319 |
ENST00000370766.8 | hg19 | chrX | 134,419,723 | 134,478,034 | 58,312 |
ENST00000370764.1 | hg19 | chrX | 134,419,724 | 134,429,959 | 10,236 |
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