SPATA13-AS1 SPATA13 antisense RNA 1
Information
- Symbol
- SPATA13-AS1
- Type
- ncRNA
- Description
- SPATA13 antisense RNA 1
- Entrez Gene ID
- 100874231
- Genome
- hg19
- Position
- chr13:24,826,887-24,828,577
- Genome
- hg38
- Position
- chr13:24,252,749-24,254,439
- HGNC
- HGNC:39905 HGNC
- Ensembl
- ENSG00000227213 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000430733.1 | hg38 | chr13 | 24,252,749 | 24,254,439 | 1,691 |
ENST00000430733.1 | hg19 | chr13 | 24,826,887 | 24,828,577 | 1,691 |
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