SNORD71 small nucleolar RNA, C/D box 71
Information
- Symbol
- SNORD71
- Type
- snoRNA
- Description
- small nucleolar RNA, C/D box 71
- Entrez Gene ID
- 692111
- Genome
- hg19
- Position
- chr16:71,792,305-71,792,390
- Genome
- hg38
- Position
- chr16:71,758,402-71,758,487
- HGNC
- HGNC:32732 HGNC
- Ensembl
- ENSG00000223224 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 |
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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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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-239 |
SYNONYM | MIRN768 |
SYNONYM | hsa-mir-768 |
HGNC | HGNC:32732 HGNC |
Ensembl | ENSG00000223224 Ensembl |
AllianceGenome | HGNC:32732 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000411292.1 | hg38 | chr16 | 71,758,402 | 71,758,487 | 86 |
ENST00000411292.1 | hg19 | chr16 | 71,792,305 | 71,792,390 | 86 |
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