MIR3591 microRNA 3591
Information
- Symbol
- MIR3591
- Type
- ncRNA
- Description
- microRNA 3591
- Entrez Gene ID
- 100616357
- Genome
- hg19
- Position
- chr18:56,118,306-56,118,390
- Genome
- hg38
- Position
- chr18:58,451,080-58,451,152
- HGNC
- HGNC:41875 HGNC
- Ensembl
- ENSG00000207778 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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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:41875 HGNC |
Ensembl | ENSG00000207778 Ensembl |
miRBase | MI0017383 |
AllianceGenome | HGNC:41875 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000636727.1 | hg38 | chr18 | 58,451,080 | 58,451,152 | 73 |
ENST00000385044.1 | hg19 | chr18 | 56,118,306 | 56,118,390 | 85 |
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