ATXN8OS ATXN8 opposite strand lncRNA
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 | KLHL1AS |
SYNONYM | NCRNA00003 |
SYNONYM | SCA8 |
MIM | 603680 OMIM |
HGNC | HGNC:10561 HGNC |
Ensembl | ENSG00000230223 Ensembl |
AllianceGenome | HGNC:10561 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000414504.6 | hg38 | chr13 | 70,107,213 | 70,139,429 | 32,217 |
ENST00000660386.1 | hg38 | chr13 | 70,107,829 | 70,149,092 | 41,264 |
ENST00000677785.1 | hg38 | chr13 | 70,108,355 | 70,165,104 | 56,750 |
ENST00000678624.1 | hg38 | chr13 | 70,107,780 | 70,171,738 | 63,959 |
ENST00000414504.6 | hg19 | chr13 | 70,681,345 | 70,713,561 | 32,217 |
ENST00000678624.1 | hg19 | chr13 | 70,681,912 | 70,745,870 | 63,959 |
ENST00000660386.1 | hg19 | chr13 | 70,681,961 | 70,723,224 | 41,264 |
ENST00000677785.1 | hg19 | chr13 | 70,682,487 | 70,739,236 | 56,750 |
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