BORA BORA aurora kinase A activator
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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66 |
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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 |
Search Word
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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 | C13orf34 |
MIM | 610510 OMIM |
HGNC | HGNC:24724 HGNC |
Ensembl | ENSG00000136122 Ensembl |
AllianceGenome | HGNC:24724 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000390667.11 | hg38 | chr13 | 72,727,923 | 72,756,196 | 28,274 |
ENST00000613797.4 | hg38 | chr13 | 72,727,904 | 72,756,198 | 28,295 |
ENST00000651477.1 | hg38 | chr13 | 72,727,904 | 72,755,449 | 27,546 |
ENST00000652266.1 | hg38 | chr13 | 72,727,749 | 72,756,198 | 28,450 |
ENST00000652266.1 | hg19 | chr13 | 73,301,887 | 73,330,336 | 28,450 |
ENST00000651477.1 | hg19 | chr13 | 73,302,042 | 73,329,587 | 27,546 |
ENST00000613797.4 | hg19 | chr13 | 73,302,042 | 73,330,336 | 28,295 |
ENST00000390667.11 | hg19 | chr13 | 73,302,061 | 73,330,334 | 28,274 |
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