CNTNAP2-AS1 CNTNAP2 antisense RNA 1
Information
- Symbol
- CNTNAP2-AS1
- Type
- ncRNA
- Description
- CNTNAP2 antisense RNA 1
- Entrez Gene ID
- 101928700
- Genome
- hg19
- Position
- chr7:146,778,026-146,794,701
- Genome
- hg38
- Position
- chr7:147,080,934-147,097,609
- HGNC
- HGNC:40657 HGNC
- Ensembl
- ENSG00000236795 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
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not provided | 1 | 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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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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ENST00000434887.1 | hg38 | chr7 | 147,080,934 | 147,097,609 | 16,676 |
ENST00000434887.1 | hg19 | chr7 | 146,778,026 | 146,794,701 | 16,676 |
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