CCDC92 coiled-coil domain containing 92
Information
- Symbol
- CCDC92
- Type
- protein-coding
- Description
- coiled-coil domain containing 92
- Entrez Gene ID
- 80212
- Genome
- hg19
- Position
- chr12:124,420,173-124,457,378
- Genome
- hg38
- Position
- chr12:123,935,626-123,972,831
- HGNC
- HGNC:29563 HGNC
- Ensembl
- ENSG00000119242 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
52 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000545891.5 | hg38 | chr12 | 123,936,436 | 123,972,734 | 36,299 |
| ENST00000238156.8 | hg38 | chr12 | 123,935,626 | 123,972,831 | 37,206 |
| ENST00000545135.5 | hg38 | chr12 | 123,936,417 | 123,946,773 | 10,357 |
| ENST00000238156.8 | hg19 | chr12 | 124,420,173 | 124,457,378 | 37,206 |
| ENST00000545135.5 | hg19 | chr12 | 124,420,964 | 124,431,320 | 10,357 |
| ENST00000545891.5 | hg19 | chr12 | 124,420,983 | 124,457,281 | 36,299 |
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