MIR4513 microRNA 4513
Information
- Symbol
- MIR4513
- Type
- ncRNA
- Description
- microRNA 4513
- Entrez Gene ID
- 100616183
- Genome
- hg19
- Position
- chr15:75,081,013-75,081,098
- Genome
- hg38
- Position
- chr15:74,788,672-74,788,757
- HGNC
- HGNC:41855 HGNC
- Ensembl
- ENSG00000264386 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
Ranking
ClinVar | |
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0 |
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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
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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Category | : |
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Filtering | : |
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 |
---|---|
HGNC | HGNC:41855 HGNC |
Ensembl | ENSG00000264386 Ensembl |
miRBase | MI0016879 |
AllianceGenome | HGNC:41855 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000581077.1 | hg38 | chr15 | 74,788,672 | 74,788,757 | 86 |
ENST00000581077.1 | hg19 | chr15 | 75,081,013 | 75,081,098 | 86 |
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