CDK4 cyclin dependent kinase 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 1 | 6 |
Likely pathogenic | 0 | 4 |
Benign | 11 | 56 |
Likely benign | 3 | 750 |
Conflicting classifications of pathogenicity | 0 | 88 |
not provided | 81 | 0 |
Uncertain significance | 40 | 1,154 |
Ranking
ClinVar | |
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0 |
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0 |
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686 |
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1,258 |
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8 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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Variants
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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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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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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 | CMM3 |
SYNONYM | PSK-J3 |
MIM | 123829 OMIM |
HGNC | HGNC:1773 HGNC |
Ensembl | ENSG00000135446 Ensembl |
AllianceGenome | HGNC:1773 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000312990.10 | hg38 | chr12 | 57,747,727 | 57,752,447 | 4,721 |
ENST00000257904.11 | hg38 | chr12 | 57,747,727 | 57,752,310 | 4,584 |
ENST00000549606.5 | hg38 | chr12 | 57,748,426 | 57,752,353 | 3,928 |
ENST00000257904.11 | hg19 | chr12 | 58,141,510 | 58,146,093 | 4,584 |
ENST00000312990.10 | hg19 | chr12 | 58,141,510 | 58,146,230 | 4,721 |
ENST00000549606.5 | hg19 | chr12 | 58,142,209 | 58,146,136 | 3,928 |
Key | Value |
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strand | - |
start | 58,141,509 |
Gene Symbol | CDK4 |
Entrez GeneId | 1,019 |
Chr Band | 12q14 |
end | 58,146,229 |
chr | chr12 |
Name | cyclin-dependent kinase 4 |
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