WT1-AS WT1 antisense RNA
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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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 | WIT-1 |
SYNONYM | WIT1 |
SYNONYM | WT1-AS1 |
SYNONYM | WT1AS |
MIM | 607899 OMIM |
HGNC | HGNC:18135 HGNC |
Ensembl | ENSG00000183242 Ensembl |
AllianceGenome | HGNC:18135 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000525436.1 | hg38 | chr11 | 32,435,801 | 32,458,769 | 22,969 |
ENST00000690579.1 | hg38 | chr11 | 32,435,622 | 32,500,632 | 65,011 |
ENST00000395900.1 | hg38 | chr11 | 32,435,579 | 32,441,404 | 5,826 |
ENST00000702558.1 | hg38 | chr11 | 32,435,616 | 32,454,276 | 18,661 |
ENST00000494911.5 | hg38 | chr11 | 32,435,518 | 32,438,707 | 3,190 |
ENST00000494911.5 | hg19 | chr11 | 32,457,064 | 32,460,253 | 3,190 |
ENST00000395900.1 | hg19 | chr11 | 32,457,125 | 32,462,950 | 5,826 |
ENST00000702558.1 | hg19 | chr11 | 32,457,162 | 32,475,822 | 18,661 |
ENST00000690579.1 | hg19 | chr11 | 32,457,168 | 32,522,178 | 65,011 |
ENST00000525436.1 | hg19 | chr11 | 32,457,347 | 32,480,315 | 22,969 |
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