CT47A8 cancer/testis antigen family 47 member A8
Information
- Symbol
- CT47A8
- Type
- protein-coding
- Description
- cancer/testis antigen family 47 member A8
- Entrez Gene ID
- 728049
- Genome
- hg19
- Position
- chrX:120,082,276-120,085,598
- Genome
- hg38
- Position
- chrX:120,948,422-120,951,744
- MIM
- 300787 OMIM
- HGNC
- HGNC:33289 HGNC
- Ensembl
- ENSG00000230347 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Ranking
ClinVar | |
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Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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Search word | : | |
Filtering | : |
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 |
Type | ID |
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SYNONYM | CT47.8 |
MIM | 300787 OMIM |
HGNC | HGNC:33289 HGNC |
Ensembl | ENSG00000230347 Ensembl |
AllianceGenome | HGNC:33289 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000457977.3 | hg38 | chrX | 120,948,422 | 120,951,744 | 3,323 |
ENST00000457977.3 | hg19 | chrX | 120,082,276 | 120,085,598 | 3,323 |
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