MIR4744 microRNA 4744
Information
- Symbol
- MIR4744
- Type
- ncRNA
- Description
- microRNA 4744
- Entrez Gene ID
- 100616420
- Genome
- hg19
- Position
- chr18:46,576,057-46,576,138
- Genome
- hg38
- Position
- chr18:49,049,687-49,049,768
- HGNC
- HGNC:41866 HGNC
- Ensembl
- ENSG00000263849 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:41866 HGNC |
Ensembl | ENSG00000263849 Ensembl |
miRBase | MI0017382 |
AllianceGenome | HGNC:41866 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000581563.1 | hg38 | chr18 | 49,049,687 | 49,049,768 | 82 |
ENST00000581563.1 | hg19 | chr18 | 46,576,057 | 46,576,138 | 82 |
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