CCDC42 coiled-coil domain containing 42
Information
- Symbol
- CCDC42
- Type
- protein-coding
- Description
- coiled-coil domain containing 42
- Entrez Gene ID
- 146849
- Genome
- hg19
- Position
- chr17:8,633,253-8,648,154
- Genome
- hg38
- Position
- chr17:8,729,935-8,744,836
- HGNC
- HGNC:26528 HGNC
- Ensembl
- ENSG00000161973 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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 |
Search Word
Target data | : |
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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Filtering | : |
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 | CCDC42A |
HGNC | HGNC:26528 HGNC |
Ensembl | ENSG00000161973 Ensembl |
AllianceGenome | HGNC:26528 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000539522.2 | hg38 | chr17 | 8,729,950 | 8,744,787 | 14,838 |
ENST00000293845.8 | hg38 | chr17 | 8,729,935 | 8,744,836 | 14,902 |
ENST00000293845.8 | hg19 | chr17 | 8,633,253 | 8,648,154 | 14,902 |
ENST00000539522.2 | hg19 | chr17 | 8,633,268 | 8,648,105 | 14,838 |
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