CCNP cyclin P
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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42 |
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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 |
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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 | CNTD2 |
MIM | 620396 OMIM |
HGNC | HGNC:25805 HGNC |
Ensembl | ENSG00000105219 Ensembl |
AllianceGenome | HGNC:25805 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000599263.6 | hg38 | chr19 | 40,222,208 | 40,226,697 | 4,490 |
ENST00000430325.7 | hg38 | chr19 | 40,222,208 | 40,226,689 | 4,482 |
ENST00000513948.1 | hg38 | chr19 | 40,223,048 | 40,224,937 | 1,890 |
ENST00000430325.7 | hg19 | chr19 | 40,728,115 | 40,732,596 | 4,482 |
ENST00000599263.6 | hg19 | chr19 | 40,728,115 | 40,732,604 | 4,490 |
ENST00000513948.1 | hg19 | chr19 | 40,728,955 | 40,730,844 | 1,890 |
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