GNAS-AS1 GNAS antisense RNA 1
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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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 | GNAS-AS |
SYNONYM | GNAS1AS |
SYNONYM | GNASAS |
SYNONYM | NCRNA00075 |
SYNONYM | NESP-AS |
SYNONYM | NESPAS |
SYNONYM | SANG |
MIM | 610540 OMIM |
HGNC | HGNC:24872 HGNC |
Ensembl | ENSG00000235590 Ensembl |
AllianceGenome | HGNC:24872 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000424094.6 | hg38 | chr20 | 58,818,919 | 58,850,903 | 31,985 |
ENST00000443966.2 | hg38 | chr20 | 58,826,736 | 58,840,844 | 14,109 |
ENST00000701893.1 | hg38 | chr20 | 58,818,926 | 58,850,890 | 31,965 |
ENST00000424094.6 | hg19 | chr20 | 57,393,974 | 57,425,958 | 31,985 |
ENST00000701893.1 | hg19 | chr20 | 57,393,981 | 57,425,945 | 31,965 |
ENST00000443966.2 | hg19 | chr20 | 57,401,791 | 57,415,899 | 14,109 |
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