CT69 cancer/testis associated transcript 69
Information
- Symbol
- CT69
- Type
- ncRNA
- Description
- cancer/testis associated transcript 69
- Entrez Gene ID
- 101928231
- Genome
- hg19
- Position
- chr6:134,749,377-134,796,638
- Genome
- hg38
- Position
- chr6:134,428,239-134,475,500
- HGNC
- HGNC:37196 HGNC
- Ensembl
- ENSG00000231971 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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
[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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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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ENST00000668601.1 | hg38 | chr6 | 134,436,526 | 134,476,554 | 40,029 |
ENST00000657570.1 | hg38 | chr6 | 134,428,239 | 134,475,500 | 47,262 |
ENST00000660051.1 | hg38 | chr6 | 134,428,243 | 134,476,565 | 48,323 |
ENST00000657570.1 | hg19 | chr6 | 134,749,377 | 134,796,638 | 47,262 |
ENST00000660051.1 | hg19 | chr6 | 134,749,381 | 134,797,703 | 48,323 |
ENST00000668601.1 | hg19 | chr6 | 134,757,664 | 134,797,692 | 40,029 |
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