ZNF140 zinc finger protein 140
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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
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 | pHZ-39 |
MIM | 604082 OMIM |
HGNC | HGNC:12925 HGNC |
Ensembl | ENSG00000196387 Ensembl |
AllianceGenome | HGNC:12925 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000319849.7 | hg38 | chr12 | 133,080,932 | 133,105,590 | 24,659 |
ENST00000440550.6 | hg38 | chr12 | 133,080,932 | 133,106,866 | 25,935 |
ENST00000544426.5 | hg38 | chr12 | 133,080,882 | 133,107,526 | 26,645 |
ENST00000355557.7 | hg38 | chr12 | 133,080,923 | 133,107,428 | 26,506 |
ENST00000544426.5 | hg19 | chr12 | 133,657,468 | 133,684,112 | 26,645 |
ENST00000355557.7 | hg19 | chr12 | 133,657,509 | 133,684,014 | 26,506 |
ENST00000319849.7 | hg19 | chr12 | 133,657,518 | 133,682,176 | 24,659 |
ENST00000440550.6 | hg19 | chr12 | 133,657,518 | 133,683,452 | 25,935 |
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