MIR302B microRNA 302b
Clinical Significance
MGeND | ClinVar |
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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 | MIRN302B |
SYNONYM | mir-302b |
MIM | 614597 OMIM |
HGNC | HGNC:31763 HGNC |
Ensembl | ENSG00000284463 Ensembl |
miRBase | MI0000772 |
AllianceGenome | HGNC:31763 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000362188.1 | hg38 | chr4 | 112,648,485 | 112,648,557 | 73 |
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