MIR509-3 microRNA 509-3
Clinical Significance
MGeND | ClinVar | |
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not provided | 6 | 0 |
Ranking
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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Target data | : |
MGeND data only
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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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SYNONYM | MIRN509-3 |
SYNONYM | mir-509-3 |
MIM | 300876 OMIM |
HGNC | HGNC:33675 HGNC |
Ensembl | ENSG00000212014 Ensembl |
miRBase | MI0005717 |
AllianceGenome | HGNC:33675 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000390725.1 | hg38 | chrX | 147,259,652 | 147,259,726 | 75 |
ENST00000390725.1 | hg19 | chrX | 146,341,170 | 146,341,244 | 75 |
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