RHOXF1-AS1 RHOXF1 antisense RNA 1
Information
- Symbol
- RHOXF1-AS1
- Type
- ncRNA
- Description
- RHOXF1 antisense RNA 1
- Entrez Gene ID
- 101928969
- Genome
- hg19
- Position
- chrX:119,170,201-119,280,760
- Genome
- hg38
- Position
- chrX:120,036,236-120,146,854
- HGNC
- HGNC:51582 HGNC
- Ensembl
- ENSG00000258545 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000553843.5 | hg38 | chrX | 120,036,236 | 120,146,854 | 110,619 |
ENST00000553843.5 | hg19 | chrX | 119,170,201 | 119,280,760 | 110,560 |
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