HIC2 HIC ZBTB transcriptional repressor 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 90 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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96 |
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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 | HRG22 |
SYNONYM | ZBTB30 |
SYNONYM | ZNF907 |
MIM | 607712 OMIM |
HGNC | HGNC:18595 HGNC |
Ensembl | ENSG00000169635 Ensembl |
AllianceGenome | HGNC:18595 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000407598.2 | hg38 | chr22 | 21,420,636 | 21,449,434 | 28,799 |
ENST00000443632.2 | hg38 | chr22 | 21,442,460 | 21,451,463 | 9,004 |
ENST00000407464.7 | hg38 | chr22 | 21,417,371 | 21,451,463 | 34,093 |
ENST00000407464.7 | hg19 | chr22 | 21,771,660 | 21,805,752 | 34,093 |
ENST00000407598.2 | hg19 | chr22 | 21,774,925 | 21,803,723 | 28,799 |
ENST00000443632.2 | hg19 | chr22 | 21,796,749 | 21,805,752 | 9,004 |
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