C2orf73 chromosome 2 open reading frame 73
Information
- Symbol
- C2orf73
- Type
- protein-coding
- Description
- chromosome 2 open reading frame 73
- Entrez Gene ID
- 129852
- Genome
- hg19
- Position
- chr2:54,558,021-54,588,718
- Genome
- hg38
- Position
- chr2:54,330,884-54,361,581
- HGNC
- HGNC:26861 HGNC
- Ensembl
- ENSG00000177994 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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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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 |
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ENST00000398634.7 | hg38 | chr2 | 54,330,884 | 54,361,581 | 30,698 |
ENST00000615983.1 | hg38 | chr2 | 54,330,965 | 54,361,387 | 30,423 |
ENST00000405749.5 | hg38 | chr2 | 54,330,902 | 54,383,194 | 52,293 |
ENST00000398634.7 | hg19 | chr2 | 54,558,021 | 54,588,718 | 30,698 |
ENST00000405749.5 | hg19 | chr2 | 54,558,039 | 54,610,331 | 52,293 |
ENST00000615983.1 | hg19 | chr2 | 54,558,102 | 54,588,524 | 30,423 |
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