MIR17HG miR-17-92a-1 cluster host gene
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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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 | LINC00048 |
SYNONYM | MIHG1 |
SYNONYM | MIRH1 |
SYNONYM | MIRHG1 |
SYNONYM | NCRNA00048 |
SYNONYM | miR-17-92 |
MIM | 609415 OMIM |
HGNC | HGNC:23564 HGNC |
Ensembl | ENSG00000215417 Ensembl |
AllianceGenome | HGNC:23564 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000710422.1 | hg38 | chr13 | 91,347,697 | 91,397,592 | 49,896 |
ENST00000582141.6 | hg38 | chr13 | 91,347,820 | 91,355,068 | 7,249 |
ENST00000710414.1 | hg38 | chr13 | 91,352,334 | 91,365,107 | 12,774 |
ENST00000710422.1 | hg19 | chr13 | 91,999,951 | 92,049,846 | 49,896 |
ENST00000582141.6 | hg19 | chr13 | 92,000,074 | 92,007,322 | 7,249 |
ENST00000710414.1 | hg19 | chr13 | 92,004,588 | 92,017,361 | 12,774 |
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