MIR548V microRNA 548v
Information
- Symbol
- MIR548V
- Type
- ncRNA
- Description
- microRNA 548v
- Entrez Gene ID
- 100422850
- Genome
- hg19
- Position
- chr8:17,539,087-17,539,166
- Genome
- hg38
- Position
- chr8:17,681,578-17,681,657
- HGNC
- HGNC:38302 HGNC
- Ensembl
- ENSG00000265520 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 |
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 |
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 |
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HGNC | HGNC:38302 HGNC |
Ensembl | ENSG00000265520 Ensembl |
miRBase | MI0014174 |
AllianceGenome | HGNC:38302 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000584165.1 | hg38 | chr8 | 17,681,578 | 17,681,657 | 80 |
ENST00000584165.1 | hg19 | chr8 | 17,539,087 | 17,539,166 | 80 |
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