MIR532 microRNA 532
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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
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 |
Search Word
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 | MIRN532 |
SYNONYM | hsa-mir-532 |
SYNONYM | mir-532 |
MIM | 301023 OMIM |
HGNC | HGNC:32795 HGNC |
Ensembl | ENSG00000207758 Ensembl |
miRBase | MI0003205 |
AllianceGenome | HGNC:32795 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000385025.1 | hg38 | chrX | 50,003,148 | 50,003,238 | 91 |
ENST00000385025.1 | hg19 | chrX | 49,767,754 | 49,767,844 | 91 |
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