CCDC107 coiled-coil domain containing 107
Information
- Symbol
- CCDC107
- Type
- protein-coding
- Description
- coiled-coil domain containing 107
- Entrez Gene ID
- 203260
- Genome
- hg19
- Position
- chr9:35,658,289-35,661,508
- Genome
- hg38
- Position
- chr9:35,658,292-35,661,511
- HGNC
- HGNC:28465 HGNC
- Ensembl
- ENSG00000159884 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
![]() |
56 |
![]() |
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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| Filtering | : |
| 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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| Category | : |
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| Search word | : | |
| Filtering | : |
| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | PSEC0222 |
| HGNC | HGNC:28465 HGNC |
| Ensembl | ENSG00000159884 Ensembl |
| AllianceGenome | HGNC:28465 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000421582.2 | hg38 | chr9 | 35,658,317 | 35,661,403 | 3,087 |
| ENST00000378406.5 | hg38 | chr9 | 35,658,314 | 35,661,187 | 2,874 |
| ENST00000378409.7 | hg38 | chr9 | 35,658,290 | 35,661,499 | 3,210 |
| ENST00000378407.7 | hg38 | chr9 | 35,658,304 | 35,661,186 | 2,883 |
| ENST00000426546.7 | hg38 | chr9 | 35,658,292 | 35,661,511 | 3,220 |
| ENST00000327351.6 | hg38 | chr9 | 35,658,317 | 35,661,177 | 2,861 |
| ENST00000378409.7 | hg19 | chr9 | 35,658,287 | 35,661,496 | 3,210 |
| ENST00000426546.7 | hg19 | chr9 | 35,658,289 | 35,661,508 | 3,220 |
| ENST00000378407.7 | hg19 | chr9 | 35,658,301 | 35,661,183 | 2,883 |
| ENST00000378406.5 | hg19 | chr9 | 35,658,311 | 35,661,184 | 2,874 |
| ENST00000327351.6 | hg19 | chr9 | 35,658,314 | 35,661,174 | 2,861 |
| ENST00000421582.2 | hg19 | chr9 | 35,658,314 | 35,661,400 | 3,087 |
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