SNORA22B small nucleolar RNA, H/ACA box 22B
Information
- Symbol
- SNORA22B
- Type
- snoRNA
- Description
- small nucleolar RNA, H/ACA box 22B
- Entrez Gene ID
- 109616964
- Genome
- hg19
- Position
- chr7:56,123,058-56,123,195
- Genome
- hg38
- Position
- chr7:56,055,365-56,055,502
- HGNC
- HGNC:52196 HGNC
- Ensembl
- ENSG00000206603 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
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not provided | 1 | 0 |
Ranking
ClinVar | |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000383876.1 | hg38 | chr7 | 56,055,365 | 56,055,502 | 138 |
ENST00000383876.1 | hg19 | chr7 | 56,123,058 | 56,123,195 | 138 |
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