CASP4 caspase 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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
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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 |
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Target data | : |
MGeND data only
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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 | ICE(rel)II |
SYNONYM | ICEREL-II |
SYNONYM | ICH-2 |
SYNONYM | Mih1 |
SYNONYM | Mih1/TX |
SYNONYM | TX |
MIM | 602664 OMIM |
HGNC | HGNC:1505 HGNC |
Ensembl | ENSG00000196954 Ensembl |
AllianceGenome | HGNC:1505 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000444739.7 | hg38 | chr11 | 104,942,866 | 104,968,574 | 25,709 |
ENST00000393150.7 | hg38 | chr11 | 104,942,868 | 104,956,698 | 13,831 |
ENST00000444739.7 | hg19 | chr11 | 104,813,593 | 104,839,301 | 25,709 |
ENST00000393150.7 | hg19 | chr11 | 104,813,595 | 104,827,425 | 13,831 |
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