LINC00486 long intergenic non-protein coding RNA 486
Information
- Symbol
- LINC00486
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 486
- Entrez Gene ID
- 285045
- Genome
- hg19
- Position
- chr2:33,050,489-33,067,632
- Genome
- hg38
- Position
- chr2:32,825,422-32,842,565
- HGNC
- HGNC:42946 HGNC
- Ensembl
- ENSG00000230876 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000414054.5 | hg38 | chr2 | 32,825,443 | 32,926,693 | 101,251 |
| ENST00000424364.6 | hg38 | chr2 | 32,841,014 | 32,902,123 | 61,110 |
| ENST00000663772.1 | hg38 | chr2 | 32,825,422 | 32,842,565 | 17,144 |
| ENST00000657199.1 | hg38 | chr2 | 32,825,440 | 32,842,622 | 17,183 |
| ENST00000648808.2 | hg38 | chr2 | 32,825,359 | 32,842,597 | 17,239 |
| ENST00000648808.2 | hg19 | chr2 | 33,050,426 | 33,067,664 | 17,239 |
| ENST00000663772.1 | hg19 | chr2 | 33,050,489 | 33,067,632 | 17,144 |
| ENST00000657199.1 | hg19 | chr2 | 33,050,507 | 33,067,689 | 17,183 |
| ENST00000414054.5 | hg19 | chr2 | 33,050,510 | 33,151,760 | 101,251 |
| ENST00000424364.6 | hg19 | chr2 | 33,066,081 | 33,127,190 | 61,110 |
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