SNORA73B small nucleolar RNA, H/ACA box 73B
Information
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | 105A |
SYNONYM | E1c |
SYNONYM | RNU105A |
SYNONYM | RNU17B |
SYNONYM | U17B |
MIM | 603239 OMIM |
HGNC | HGNC:10116 HGNC |
Ensembl | ENSG00000200087 Ensembl |
AllianceGenome | HGNC:10116 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000363217.1 | hg38 | chr1 | 28,508,559 | 28,508,762 | 204 |
ENST00000363217.1 | hg19 | chr1 | 28,835,071 | 28,835,274 | 204 |
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