MIR4666A microRNA 4666a
Information
- Symbol
- MIR4666A
- Type
- ncRNA
- Description
- microRNA 4666a
- Entrez Gene ID
- 100616308
- Genome
- hg19
- Position
- chr1:228,649,775-228,649,853
- Genome
- hg38
- Position
- chr1:228,462,074-228,462,152
- HGNC
- HGNC:41750 HGNC
- Ensembl
- ENSG00000266174 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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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 |
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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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Category | : |
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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 | MIR4666 |
SYNONYM | hsa-mir-4666a |
HGNC | HGNC:41750 HGNC |
Ensembl | ENSG00000266174 Ensembl |
miRBase | MI0017296 |
AllianceGenome | HGNC:41750 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000580160.1 | hg38 | chr1 | 228,462,074 | 228,462,152 | 79 |
ENST00000580160.1 | hg19 | chr1 | 228,649,775 | 228,649,853 | 79 |
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