BRWD1-AS2 BRWD1 antisense RNA 2
Information
- Symbol
- BRWD1-AS2
- Type
- ncRNA
- Description
- BRWD1 antisense RNA 2
- Entrez Gene ID
- 103091865
- Genome
- hg19
- Position
- chr21:40,685,887-40,686,886
- Genome
- hg38
- Position
- chr21:39,313,907-39,314,962
- HGNC
- HGNC:16423 HGNC
- Ensembl
- ENSG00000255568 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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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 |
Type | ID |
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SYNONYM | BRWD1-IT2 |
SYNONYM | C21orf87 |
SYNONYM | NCRNA00257 |
HGNC | HGNC:16423 HGNC |
Ensembl | ENSG00000255568 Ensembl |
AllianceGenome | HGNC:16423 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000603064.3 | hg38 | chr21 | 39,313,907 | 39,314,962 | 1,056 |
ENST00000603064.1 | hg19 | chr21 | 40,685,887 | 40,686,886 | 1,000 |
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