MIR219A1 microRNA 219a-1
Clinical Significance
MGeND | ClinVar |
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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
[No Data.]
Locus Zoom
Variants
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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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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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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 | MIR219-1 |
SYNONYM | MIRN219-1 |
SYNONYM | MRI219-1 |
SYNONYM | hsa-mir-219a-1 |
SYNONYM | mir-219 |
SYNONYM | mir-219a-1 |
MIM | 611500 OMIM |
HGNC | HGNC:31597 HGNC |
Ensembl | ENSG00000199036 Ensembl |
miRBase | MI0000296 |
AllianceGenome | HGNC:31597 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000362166.1 | hg38 | chr6 | 33,207,835 | 33,207,944 | 110 |
ENST00000362166.1 | hg19 | chr6 | 33,175,612 | 33,175,721 | 110 |
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