CCDC121 coiled-coil domain containing 121
Information
- Symbol
- CCDC121
- Type
- protein-coding
- Description
- coiled-coil domain containing 121
- Entrez Gene ID
- 79635
- Genome
- hg19
- Position
- chr2:27,849,796-27,851,745
- Genome
- hg38
- Position
- chr2:27,626,929-27,628,878
- HGNC
- HGNC:25833 HGNC
- Ensembl
- ENSG00000176714 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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54 |
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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 |
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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 |
---|---|---|---|---|---|
ENST00000324364.4 | hg38 | chr2 | 27,625,638 | 27,629,012 | 3,375 |
ENST00000394775.3 | hg38 | chr2 | 27,626,929 | 27,628,878 | 1,950 |
ENST00000324364.4 | hg19 | chr2 | 27,848,505 | 27,851,879 | 3,375 |
ENST00000394775.3 | hg19 | chr2 | 27,849,796 | 27,851,745 | 1,950 |
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