SCN1A-AS1 SCN1A and SCN9A antisense RNA 1
Information
- Symbol
- SCN1A-AS1
- Type
- ncRNA
- Description
- SCN1A and SCN9A antisense RNA 1
- Entrez Gene ID
- 101929680
- Genome
- hg19
- Position
- chr2:167,005,730-167,165,060
- Genome
- hg38
- Position
- chr2:166,149,220-166,308,550
- HGNC
- HGNC:54069 HGNC
- Ensembl
- ENSG00000236107 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 16 | 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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Category | : |
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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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Category | : |
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Search word | : | |
Filtering | : |
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000651574.1 | hg38 | chr2 | 165,957,401 | 166,352,930 | 395,530 |
ENST00000651562.1 | hg38 | chr2 | 165,957,421 | 166,061,677 | 104,257 |
ENST00000668610.1 | hg38 | chr2 | 166,149,263 | 166,308,494 | 159,232 |
ENST00000447809.2 | hg38 | chr2 | 166,081,531 | 166,301,784 | 220,254 |
ENST00000595268.3 | hg38 | chr2 | 166,015,680 | 166,060,458 | 44,779 |
ENST00000651782.1 | hg38 | chr2 | 166,149,220 | 166,308,550 | 159,331 |
ENST00000657189.1 | hg38 | chr2 | 166,149,177 | 166,300,208 | 151,032 |
ENST00000668514.1 | hg38 | chr2 | 166,149,220 | 166,296,981 | 147,762 |
ENST00000651673.1 | hg38 | chr2 | 165,957,418 | 166,062,783 | 105,366 |
ENST00000651013.1 | hg38 | chr2 | 166,149,181 | 166,390,771 | 241,591 |
ENST00000447809.2 | hg19 | chr2 | 166,938,041 | 167,158,294 | 220,254 |
ENST00000595268.3 | hg19 | chr2 | 166,872,190 | 166,916,968 | 44,779 |
ENST00000651562.1 | hg19 | chr2 | 166,813,931 | 166,918,187 | 104,257 |
ENST00000651574.1 | hg19 | chr2 | 166,813,911 | 167,209,440 | 395,530 |
ENST00000651673.1 | hg19 | chr2 | 166,813,928 | 166,919,293 | 105,366 |
ENST00000657189.1 | hg19 | chr2 | 167,005,687 | 167,156,718 | 151,032 |
ENST00000651013.1 | hg19 | chr2 | 167,005,691 | 167,247,281 | 241,591 |
ENST00000668514.1 | hg19 | chr2 | 167,005,730 | 167,153,491 | 147,762 |
ENST00000651782.1 | hg19 | chr2 | 167,005,730 | 167,165,060 | 159,331 |
ENST00000668610.1 | hg19 | chr2 | 167,005,773 | 167,165,004 | 159,232 |
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