RBM26-AS1 RBM26 antisense RNA 1
Information
- Symbol
- RBM26-AS1
- Type
- ncRNA
- Description
- RBM26 antisense RNA 1
- Entrez Gene ID
- 100505538
- Genome
- hg19
- Position
- chr13:79,980,436-80,001,452
- Genome
- hg38
- Position
- chr13:79,406,301-79,427,317
- HGNC
- HGNC:39805 HGNC
- Ensembl
- ENSG00000227354 Ensembl
- Links
- NCBI Gene Cards OncoKB
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 |
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 | : | |
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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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ENST00000656024.1 | hg38 | chr13 | 79,406,301 | 79,427,317 | 21,017 |
ENST00000664699.1 | hg38 | chr13 | 79,406,306 | 79,425,753 | 19,448 |
ENST00000606049.1 | hg38 | chr13 | 79,406,348 | 79,424,328 | 17,981 |
ENST00000654024.1 | hg38 | chr13 | 79,406,293 | 79,424,022 | 17,730 |
ENST00000654024.1 | hg19 | chr13 | 79,980,428 | 79,998,157 | 17,730 |
ENST00000656024.1 | hg19 | chr13 | 79,980,436 | 80,001,452 | 21,017 |
ENST00000664699.1 | hg19 | chr13 | 79,980,441 | 79,999,888 | 19,448 |
ENST00000606049.1 | hg19 | chr13 | 79,980,483 | 79,998,463 | 17,981 |
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