LINC00662 long intergenic non-protein coding RNA 662
Information
- Symbol
- LINC00662
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 662
- Entrez Gene ID
- 148189
- Genome
- hg19
- Position
- chr19:28,212,628-28,284,807
- Genome
- hg38
- Position
- chr19:27,721,720-27,793,899
- HGNC
- HGNC:27122 HGNC
- Ensembl
- ENSG00000261824 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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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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ENST00000659785.1 | hg38 | chr19 | 27,713,552 | 27,793,401 | 79,850 |
ENST00000665874.1 | hg38 | chr19 | 27,727,882 | 27,793,938 | 66,057 |
ENST00000657677.1 | hg38 | chr19 | 27,721,746 | 27,793,406 | 71,661 |
ENST00000671152.1 | hg38 | chr19 | 27,727,818 | 27,793,896 | 66,079 |
ENST00000666841.1 | hg38 | chr19 | 27,772,057 | 27,793,378 | 21,322 |
ENST00000590523.2 | hg38 | chr19 | 27,790,493 | 27,793,891 | 3,399 |
ENST00000661680.2 | hg38 | chr19 | 27,727,784 | 27,793,922 | 66,139 |
ENST00000666734.1 | hg38 | chr19 | 27,728,262 | 27,793,996 | 65,735 |
ENST00000655465.1 | hg38 | chr19 | 27,681,731 | 27,793,703 | 111,973 |
ENST00000658694.1 | hg38 | chr19 | 27,684,517 | 27,793,685 | 109,169 |
ENST00000656191.1 | hg38 | chr19 | 27,712,347 | 27,793,914 | 81,568 |
ENST00000670305.1 | hg38 | chr19 | 27,727,817 | 27,793,968 | 66,152 |
ENST00000654098.1 | hg38 | chr19 | 27,713,135 | 27,793,991 | 80,857 |
ENST00000666409.1 | hg38 | chr19 | 27,681,072 | 27,793,138 | 112,067 |
ENST00000664720.1 | hg38 | chr19 | 27,714,892 | 27,793,922 | 79,031 |
ENST00000668933.1 | hg38 | chr19 | 27,721,720 | 27,793,899 | 72,180 |
ENST00000656728.1 | hg38 | chr19 | 27,774,161 | 27,793,900 | 19,740 |
ENST00000657677.1 | hg19 | chr19 | 28,212,654 | 28,284,314 | 71,661 |
ENST00000661680.2 | hg19 | chr19 | 28,218,692 | 28,284,830 | 66,139 |
ENST00000655465.1 | hg19 | chr19 | 28,172,639 | 28,284,611 | 111,973 |
ENST00000654098.1 | hg19 | chr19 | 28,204,043 | 28,284,899 | 80,857 |
ENST00000656728.1 | hg19 | chr19 | 28,265,069 | 28,284,808 | 19,740 |
ENST00000658694.1 | hg19 | chr19 | 28,175,425 | 28,284,593 | 109,169 |
ENST00000656191.1 | hg19 | chr19 | 28,203,255 | 28,284,822 | 81,568 |
ENST00000659785.1 | hg19 | chr19 | 28,204,460 | 28,284,309 | 79,850 |
ENST00000666409.1 | hg19 | chr19 | 28,171,980 | 28,284,046 | 112,067 |
ENST00000590523.2 | hg19 | chr19 | 28,281,401 | 28,284,799 | 3,399 |
ENST00000664720.1 | hg19 | chr19 | 28,205,800 | 28,284,830 | 79,031 |
ENST00000666841.1 | hg19 | chr19 | 28,262,965 | 28,284,286 | 21,322 |
ENST00000668933.1 | hg19 | chr19 | 28,212,628 | 28,284,807 | 72,180 |
ENST00000670305.1 | hg19 | chr19 | 28,218,725 | 28,284,876 | 66,152 |
ENST00000671152.1 | hg19 | chr19 | 28,218,726 | 28,284,804 | 66,079 |
ENST00000665874.1 | hg19 | chr19 | 28,218,790 | 28,284,846 | 66,057 |
ENST00000666734.1 | hg19 | chr19 | 28,219,170 | 28,284,904 | 65,735 |
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