MIR92A1 microRNA 92a-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
Disease area statistics
[No Data.]
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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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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 | C13orf25 |
SYNONYM | MIR17HG |
SYNONYM | MIR92-1 |
SYNONYM | MIRH1 |
SYNONYM | MIRHG1 |
SYNONYM | MIRN92-1 |
SYNONYM | MIRN92A-1 |
SYNONYM | MIRN92A1 |
SYNONYM | miRNA92-1 |
SYNONYM | mir-92a-1 |
MIM | 609422 OMIM |
HGNC | HGNC:31643 HGNC |
Ensembl | ENSG00000283705 Ensembl |
miRBase | MI0000093 |
AllianceGenome | HGNC:31643 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000385233.3 | hg38 | chr13 | 91,351,314 | 91,351,391 | 78 |
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