MIR3612 microRNA 3612
Information
- Symbol
- MIR3612
- Type
- ncRNA
- Description
- microRNA 3612
- Entrez Gene ID
- 100500817
- Genome
- hg19
- Position
- chr12:128,778,637-128,778,723
- Genome
- hg38
- Position
- chr12:128,294,092-128,294,178
- HGNC
- HGNC:38951 HGNC
- Ensembl
- ENSG00000265635 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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0 |
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
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 |
Search Word
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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Category | : |
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Search word | : | |
Filtering | : |
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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HGNC | HGNC:38951 HGNC |
Ensembl | ENSG00000265635 Ensembl |
miRBase | MI0016002 |
AllianceGenome | HGNC:38951 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000579753.1 | hg38 | chr12 | 128,294,092 | 128,294,178 | 87 |
ENST00000579753.1 | hg19 | chr12 | 128,778,637 | 128,778,723 | 87 |
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