RNVU1-7 RNA, variant U1 small nuclear 7
Information
- Symbol
- RNVU1-7
- Type
- snRNA
- Description
- RNA, variant U1 small nuclear 7
- Entrez Gene ID
- 26864
- Genome
- hg19
- Position
- chr1:147,511,004-147,511,167
- Genome
- hg38
- Position
- chr1:148,038,753-148,038,916
- HGNC
- HGNC:37500 HGNC
- Ensembl
- ENSG00000206585 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 4 | 0 |
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
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 |
---|---|
SYNONYM | RNU1-26P |
SYNONYM | RNU1-6 |
SYNONYM | RNU1-6P |
SYNONYM | RNU1-9 |
SYNONYM | RNU1-9P |
SYNONYM | RNVU1-9 |
SYNONYM | vU1.7 |
SYNONYM | vU1.9 |
HGNC | HGNC:37500 HGNC |
Ensembl | ENSG00000206585 Ensembl |
AllianceGenome | HGNC:37500 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000383858.1 | hg38 | chr1 | 148,038,753 | 148,038,916 | 164 |
ENST00000383858.1 | hg19 | chr1 | 147,511,004 | 147,511,167 | 164 |
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