CCDC142 coiled-coil domain containing 142
Information
- Symbol
- CCDC142
- Type
- protein-coding
- Description
- coiled-coil domain containing 142
- Entrez Gene ID
- 84865
- Genome
- hg19
- Position
- chr2:74,699,959-74,710,140
- Genome
- hg38
- Position
- chr2:74,472,832-74,483,013
- HGNC
- HGNC:25889 HGNC
- Ensembl
- ENSG00000135637 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 90 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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98 |
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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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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 |
---|---|---|---|---|---|
ENST00000393965.8 | hg38 | chr2 | 74,472,832 | 74,482,998 | 10,167 |
ENST00000715459.1 | hg38 | chr2 | 74,472,832 | 74,483,013 | 10,182 |
ENST00000290418.4 | hg38 | chr2 | 74,474,102 | 74,482,996 | 8,895 |
ENST00000393965.8 | hg19 | chr2 | 74,699,959 | 74,710,125 | 10,167 |
ENST00000715459.1 | hg19 | chr2 | 74,699,959 | 74,710,140 | 10,182 |
ENST00000290418.4 | hg19 | chr2 | 74,701,229 | 74,710,123 | 8,895 |
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