SNORD89 small nucleolar RNA, C/D box 89
Information
- Symbol
- SNORD89
- Type
- snoRNA
- Description
- small nucleolar RNA, C/D box 89
- Entrez Gene ID
- 692205
- Genome
- hg19
- Position
- chr2:101,889,398-101,889,511
- Genome
- hg38
- Position
- chr2:101,272,936-101,273,049
- HGNC
- HGNC:32750 HGNC
- Ensembl
- ENSG00000212283 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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0 |
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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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 |
Type | ID |
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SYNONYM | HBII-289 |
HGNC | HGNC:32750 HGNC |
Ensembl | ENSG00000212283 Ensembl |
AllianceGenome | HGNC:32750 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000390981.1 | hg38 | chr2 | 101,272,936 | 101,273,049 | 114 |
ENST00000390981.1 | hg19 | chr2 | 101,889,398 | 101,889,511 | 114 |
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