VSTM2A-OT1 VSTM2A overlapping transcript 1
Information
- Symbol
- VSTM2A-OT1
- Type
- ncRNA
- Description
- VSTM2A overlapping transcript 1
- Entrez Gene ID
- 285878
- Genome
- hg19
- Position
- chr7:54,624,663-54,639,419
- Genome
- hg38
- Position
- chr7:54,556,970-54,571,726
- HGNC
- HGNC:50770 HGNC
- Ensembl
- ENSG00000224223 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
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not provided | 1 | 0 |
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
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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SYNONYM | GS1-18A18.1 |
HGNC | HGNC:50770 HGNC |
Ensembl | ENSG00000224223 Ensembl |
AllianceGenome | HGNC:50770 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000456049.1 | hg38 | chr7 | 54,556,970 | 54,571,726 | 14,757 |
ENST00000456049.1 | hg19 | chr7 | 54,624,663 | 54,639,419 | 14,757 |
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