SNORD116-27 small nucleolar RNA, C/D box 116-27
Information
- Symbol
- SNORD116-27
- Type
- snoRNA
- Description
- small nucleolar RNA, C/D box 116-27
- Entrez Gene ID
- 100033439
- Genome
- hg19
- Position
- chr15:25,346,722-25,346,813
- Genome
- hg38
- Position
- chr15:25,101,575-25,101,666
- HGNC
- HGNC:33093 HGNC
- Ensembl
- ENSG00000251896 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
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not provided | 2 | 0 |
Ranking
ClinVar | |
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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
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 |
Type | ID |
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SYNONYM | HBII-85-27 |
HGNC | HGNC:33093 HGNC |
Ensembl | ENSG00000251896 Ensembl |
AllianceGenome | HGNC:33093 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000516087.1 | hg38 | chr15 | 25,101,575 | 25,101,666 | 92 |
ENST00000516087.1 | hg19 | chr15 | 25,346,722 | 25,346,813 | 92 |
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