CT47C1 cancer/testis antigen family 47 member C1
Information
- Symbol
- CT47C1
- Type
- protein-coding
- Description
- cancer/testis antigen family 47 member C1
- Entrez Gene ID
- 727838
- Genome
- hg19
- Position
- chrX:118,206,956-118,210,728
- Genome
- hg38
- Position
- chrX:119,072,993-119,076,765
- HGNC
- HGNC:53820 HGNC
- Ensembl
- ENSG00000277535 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 |
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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 |
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ENST00000620151.4 | hg38 | chrX | 119,072,993 | 119,076,765 | 3,773 |
ENST00000620151.4 | hg19 | chrX | 118,206,956 | 118,210,728 | 3,773 |
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