ZNF202 zinc finger protein 202
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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58 |
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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 | ZKSCAN10 |
SYNONYM | ZSCAN42 |
MIM | 603430 OMIM |
HGNC | HGNC:12994 HGNC |
Ensembl | ENSG00000166261 Ensembl |
AllianceGenome | HGNC:12994 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000529691.1 | hg38 | chr11 | 123,724,780 | 123,741,671 | 16,892 |
ENST00000530393.6 | hg38 | chr11 | 123,723,914 | 123,741,660 | 17,747 |
ENST00000336139.8 | hg38 | chr11 | 123,724,177 | 123,741,670 | 17,494 |
ENST00000530393.6 | hg19 | chr11 | 123,594,622 | 123,612,368 | 17,747 |
ENST00000336139.8 | hg19 | chr11 | 123,594,885 | 123,612,378 | 17,494 |
ENST00000529691.1 | hg19 | chr11 | 123,595,488 | 123,612,379 | 16,892 |
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