CCDC60 coiled-coil domain containing 60
Information
- Symbol
- CCDC60
- Type
- protein-coding
- Description
- coiled-coil domain containing 60
- Entrez Gene ID
- 160777
- Genome
- hg19
- Position
- chr12:119,772,534-119,978,845
- Genome
- hg38
- Position
- chr12:119,334,729-119,541,040
- HGNC
- HGNC:28610 HGNC
- Ensembl
- ENSG00000183273 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 72 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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78 |
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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 |
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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 |
---|---|---|---|---|---|
ENST00000327554.3 | hg38 | chr12 | 119,334,729 | 119,541,040 | 206,312 |
ENST00000536742.5 | hg38 | chr12 | 119,334,712 | 119,433,636 | 98,925 |
ENST00000539847.1 | hg38 | chr12 | 119,334,929 | 119,428,925 | 93,997 |
ENST00000536742.5 | hg19 | chr12 | 119,772,517 | 119,871,441 | 98,925 |
ENST00000327554.3 | hg19 | chr12 | 119,772,534 | 119,978,845 | 206,312 |
ENST00000539847.1 | hg19 | chr12 | 119,772,734 | 119,866,730 | 93,997 |
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