SNORD116-7 small nucleolar RNA, C/D box 116-7
Information
- Symbol
- SNORD116-7
- Type
- snoRNA
- Description
- small nucleolar RNA, C/D box 116-7
- Entrez Gene ID
- 100033419
- Genome
- hg19
- Position
- chr15:25,312,935-25,313,029
- Genome
- hg38
- Position
- chr15:25,067,788-25,067,882
- HGNC
- HGNC:33073 HGNC
- Ensembl
- ENSG00000207133 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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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
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-85-7 |
HGNC | HGNC:33073 HGNC |
Ensembl | ENSG00000207133 Ensembl |
AllianceGenome | HGNC:33073 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000384404.1 | hg38 | chr15 | 25,067,788 | 25,067,882 | 95 |
ENST00000384404.1 | hg19 | chr15 | 25,312,935 | 25,313,029 | 95 |
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