RABGAP1L-DT RABGAP1L divergent transcript
Information
- Symbol
- RABGAP1L-DT
- Type
- ncRNA
- Description
- RABGAP1L divergent transcript
- Entrez Gene ID
- 102724601
- Genome
- hg19
- Position
- chr1:174,079,406-174,128,472
- Genome
- hg38
- Position
- chr1:174,110,268-174,159,334
- HGNC
- HGNC:54296 HGNC
- Ensembl
- ENSG00000227373 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 | : | |
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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ENST00000419983.5 | hg38 | chr1 | 174,115,383 | 174,160,004 | 44,622 |
ENST00000665650.1 | hg38 | chr1 | 174,110,268 | 174,159,334 | 49,067 |
ENST00000426899.6 | hg38 | chr1 | 174,113,584 | 174,160,150 | 46,567 |
ENST00000665650.1 | hg19 | chr1 | 174,079,406 | 174,128,472 | 49,067 |
ENST00000426899.6 | hg19 | chr1 | 174,082,722 | 174,129,288 | 46,567 |
ENST00000419983.5 | hg19 | chr1 | 174,084,521 | 174,129,142 | 44,622 |
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