AURKB aurora kinase B
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 5 | 0 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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34 |
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2 |
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
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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 |
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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 | AIK2 |
SYNONYM | AIM-1 |
SYNONYM | AIM1 |
SYNONYM | ARK-2 |
SYNONYM | ARK2 |
SYNONYM | AurB |
SYNONYM | IPL1 |
SYNONYM | PPP1R48 |
SYNONYM | STK-1 |
SYNONYM | STK12 |
SYNONYM | STK5 |
SYNONYM | aurkb-sv1 |
SYNONYM | aurkb-sv2 |
MIM | 604970 OMIM |
HGNC | HGNC:11390 HGNC |
Ensembl | ENSG00000178999 Ensembl |
AllianceGenome | HGNC:11390 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000534871.5 | hg38 | chr17 | 8,204,743 | 8,210,581 | 5,839 |
ENST00000578549.5 | hg38 | chr17 | 8,204,871 | 8,210,224 | 5,354 |
ENST00000316199.10 | hg38 | chr17 | 8,204,733 | 8,210,582 | 5,850 |
ENST00000585124.6 | hg38 | chr17 | 8,204,734 | 8,210,575 | 5,842 |
ENST00000316199.10 | hg19 | chr17 | 8,108,051 | 8,113,900 | 5,850 |
ENST00000585124.6 | hg19 | chr17 | 8,108,052 | 8,113,893 | 5,842 |
ENST00000534871.5 | hg19 | chr17 | 8,108,061 | 8,113,899 | 5,839 |
ENST00000578549.5 | hg19 | chr17 | 8,108,189 | 8,113,542 | 5,354 |
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