CCDC9 coiled-coil domain containing 9
Information
- Symbol
- CCDC9
- Type
- protein-coding
- Description
- coiled-coil domain containing 9
- Entrez Gene ID
- 26093
- Genome
- hg19
- Position
- chr19:47,759,782-47,775,210
- Genome
- hg38
- Position
- chr19:47,256,525-47,271,953
- HGNC
- HGNC:24560 HGNC
- Ensembl
- ENSG00000105321 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 108 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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116 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000221922.11 | hg38 | chr19 | 47,256,525 | 47,271,953 | 15,429 |
ENST00000643617.1 | hg38 | chr19 | 47,256,523 | 47,273,701 | 17,179 |
ENST00000643617.1 | hg19 | chr19 | 47,759,780 | 47,776,958 | 17,179 |
ENST00000221922.11 | hg19 | chr19 | 47,759,782 | 47,775,210 | 15,429 |
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