MESTIT1 MEST intronic transcript 1, antisense RNA
Information
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
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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 | MEST-AS1 |
SYNONYM | MEST-IT |
SYNONYM | MEST-IT1 |
SYNONYM | NCRNA00040 |
SYNONYM | PEG1-AS |
MIM | 607794 OMIM |
HGNC | HGNC:17991 HGNC |
Ensembl | ENSG00000272701 Ensembl |
AllianceGenome | HGNC:17991 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000610046.2 | hg38 | chr7 | 130,486,042 | 130,491,033 | 4,992 |
ENST00000610046.2 | hg19 | chr7 | 130,125,883 | 130,130,874 | 4,992 |
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