LINC00929 long intergenic non-protein coding RNA 929
Information
- Symbol
- LINC00929
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 929
- Entrez Gene ID
- 503519
- Genome
- hg19
- Position
- chr15:26,360,894-26,379,148
- Genome
- hg38
- Position
- chr15:26,115,747-26,134,001
- HGNC
- HGNC:48615 HGNC
- Ensembl
- ENSG00000259150 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000666709.1 | hg38 | chr15 | 26,115,747 | 26,134,001 | 18,255 |
ENST00000655889.1 | hg38 | chr15 | 26,115,784 | 26,133,023 | 17,240 |
ENST00000655889.1 | hg19 | chr15 | 26,360,931 | 26,378,170 | 17,240 |
ENST00000666709.1 | hg19 | chr15 | 26,360,894 | 26,379,148 | 18,255 |
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