C8orf58 chromosome 8 open reading frame 58
Information
- Symbol
- C8orf58
- Type
- protein-coding
- Description
- chromosome 8 open reading frame 58
- Entrez Gene ID
- 541565
- Genome
- hg19
- Position
- chr8:22,457,112-22,461,655
- Genome
- hg38
- Position
- chr8:22,599,599-22,604,142
- HGNC
- HGNC:32233 HGNC
- Ensembl
- ENSG00000241852 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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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Category | : |
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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 |
---|---|---|---|---|---|
ENST00000614574.4 | hg38 | chr8 | 22,599,601 | 22,604,150 | 4,550 |
ENST00000409586.7 | hg38 | chr8 | 22,599,601 | 22,604,133 | 4,533 |
ENST00000289989.10 | hg38 | chr8 | 22,599,599 | 22,604,142 | 4,544 |
ENST00000289989.10 | hg19 | chr8 | 22,457,112 | 22,461,655 | 4,544 |
ENST00000409586.7 | hg19 | chr8 | 22,457,114 | 22,461,646 | 4,533 |
ENST00000614574.4 | hg19 | chr8 | 22,457,114 | 22,461,663 | 4,550 |
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