RNVU1-17 RNA, variant U1 small nuclear 17
Information
- Symbol
- RNVU1-17
- Type
- snRNA
- Description
- RNA, variant U1 small nuclear 17
- Entrez Gene ID
- 101954269
- Genome
- hg19
- Position
- chr1:149,194,106-149,194,269
- Genome
- hg38
- Position
- chr1:143,699,456-143,699,619
- HGNC
- HGNC:48322 HGNC
- Ensembl
- ENSG00000207349 Ensembl
- Links
- NCBI Gene Cards OncoKB
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
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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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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Target data | : |
MGeND data only
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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 | RNU1-127 |
SYNONYM | vU1.17 |
HGNC | HGNC:48322 HGNC |
Ensembl | ENSG00000207349 Ensembl |
AllianceGenome | HGNC:48322 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000384619.1 | hg38 | chr1 | 143,699,456 | 143,699,619 | 164 |
ENST00000384619.1 | hg19 | chr1 | 149,194,106 | 149,194,269 | 164 |
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