KRBOX4 KRAB box domain containing 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 6 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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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Category | : |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
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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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | ZNF673 |
MIM | 300585 OMIM |
HGNC | HGNC:26007 HGNC |
Ensembl | ENSG00000147121 Ensembl |
AllianceGenome | HGNC:26007 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000298190.10 | hg38 | chrX | 46,447,292 | 46,473,669 | 26,378 |
ENST00000377919.6 | hg38 | chrX | 46,447,294 | 46,472,526 | 25,233 |
ENST00000487081.1 | hg38 | chrX | 46,448,233 | 46,473,594 | 25,362 |
ENST00000344302.9 | hg38 | chrX | 46,447,297 | 46,474,639 | 27,343 |
ENST00000478600.5 | hg38 | chrX | 46,447,297 | 46,497,422 | 50,126 |
ENST00000298190.10 | hg19 | chrX | 46,306,727 | 46,333,104 | 26,378 |
ENST00000377919.6 | hg19 | chrX | 46,306,729 | 46,331,961 | 25,233 |
ENST00000344302.9 | hg19 | chrX | 46,306,732 | 46,334,074 | 27,343 |
ENST00000478600.5 | hg19 | chrX | 46,306,732 | 46,356,857 | 50,126 |
ENST00000487081.1 | hg19 | chrX | 46,307,668 | 46,333,029 | 25,362 |
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