ZCCHC14-DT ZCCHC14 divergent transcript
Information
- Symbol
- ZCCHC14-DT
- Type
- ncRNA
- Description
- ZCCHC14 divergent transcript
- Entrez Gene ID
- 101928737
- Genome
- hg19
- Position
- chr16:87,526,912-87,550,546
- Genome
- hg38
- Position
- chr16:87,493,306-87,516,940
- HGNC
- HGNC:52996 HGNC
- Ensembl
- ENSG00000288568 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[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 |
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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ENST00000563921.1 | hg38 | chr16 | 87,494,187 | 87,515,635 | 21,449 |
ENST00000657113.1 | hg38 | chr16 | 87,493,306 | 87,516,940 | 23,635 |
ENST00000657113.1 | hg19 | chr16 | 87,526,912 | 87,550,546 | 23,635 |
ENST00000563921.1 | hg19 | chr16 | 87,527,793 | 87,549,241 | 21,449 |
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