CDC16 cell division cycle 16
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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72 |
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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
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 |
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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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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 | ANAPC6 |
SYNONYM | APC6 |
SYNONYM | CDC16Hs |
SYNONYM | CUT9 |
MIM | 603461 OMIM |
HGNC | HGNC:1720 HGNC |
Ensembl | ENSG00000130177 Ensembl |
AllianceGenome | HGNC:1720 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000356221.8 | hg38 | chr13 | 114,234,897 | 114,272,723 | 37,827 |
ENST00000252458.6 | hg38 | chr13 | 114,235,081 | 114,272,723 | 37,643 |
ENST00000628084.2 | hg38 | chr13 | 114,234,887 | 114,272,675 | 37,789 |
ENST00000375308.5 | hg38 | chr13 | 114,235,061 | 114,272,675 | 37,615 |
ENST00000252457.9 | hg38 | chr13 | 114,235,061 | 114,272,675 | 37,615 |
ENST00000375310.5 | hg38 | chr13 | 114,234,979 | 114,272,675 | 37,697 |
ENST00000360383.7 | hg38 | chr13 | 114,234,887 | 114,272,675 | 37,789 |
ENST00000360383.7 | hg19 | chr13 | 115,000,362 | 115,038,150 | 37,789 |
ENST00000628084.2 | hg19 | chr13 | 115,000,362 | 115,038,150 | 37,789 |
ENST00000356221.8 | hg19 | chr13 | 115,000,372 | 115,038,198 | 37,827 |
ENST00000375310.5 | hg19 | chr13 | 115,000,454 | 115,038,150 | 37,697 |
ENST00000252457.9 | hg19 | chr13 | 115,000,536 | 115,038,150 | 37,615 |
ENST00000375308.5 | hg19 | chr13 | 115,000,536 | 115,038,150 | 37,615 |
ENST00000252458.6 | hg19 | chr13 | 115,000,556 | 115,038,198 | 37,643 |
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