CT47A7 cancer/testis antigen family 47 member A7
Information
- Symbol
- CT47A7
- Type
- protein-coding
- Description
- cancer/testis antigen family 47 member A7
- Entrez Gene ID
- 653282
- Genome
- hg19
- Position
- chrX:120,087,136-120,090,454
- Genome
- hg38
- Position
- chrX:120,953,282-120,956,600
- MIM
- 300786 OMIM
- HGNC
- HGNC:33288 HGNC
- Ensembl
- ENSG00000228517 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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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
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 | CT47.7 |
MIM | 300786 OMIM |
HGNC | HGNC:33288 HGNC |
Ensembl | ENSG00000228517 Ensembl |
AllianceGenome | HGNC:33288 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000434883.3 | hg38 | chrX | 120,953,282 | 120,956,600 | 3,319 |
ENST00000434883.3 | hg19 | chrX | 120,087,136 | 120,090,454 | 3,319 |
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