MEF2C-AS2 MEF2C antisense RNA 2
Information
- Symbol
- MEF2C-AS2
- Type
- ncRNA
- Description
- MEF2C antisense RNA 2
- Entrez Gene ID
- 109729137
- Genome
- hg19
- Position
- chr5:87,971,858-88,063,294
- Genome
- hg38
- Position
- chr5:88,676,040-88,767,477
- HGNC
- HGNC:53115 HGNC
- Ensembl
- ENSG00000245864 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 |
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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000659116.1 | hg38 | chr5 | 88,676,040 | 88,767,477 | 91,438 |
ENST00000686200.1 | hg38 | chr5 | 88,676,169 | 88,691,756 | 15,588 |
ENST00000510274.1 | hg38 | chr5 | 88,676,218 | 88,722,831 | 46,614 |
ENST00000659116.1 | hg19 | chr5 | 87,971,858 | 88,063,294 | 91,437 |
ENST00000686200.1 | hg19 | chr5 | 87,971,987 | 87,987,573 | 15,587 |
ENST00000510274.1 | hg19 | chr5 | 87,972,036 | 88,018,648 | 46,613 |
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