LINC01192 long intergenic non-protein coding RNA 1192
Information
- Symbol
- LINC01192
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1192
- Entrez Gene ID
- 647107
- Genome
- hg19
- Position
- chr3:162,933,423-163,022,561
- Genome
- hg38
- Position
- chr3:163,215,635-163,304,773
- HGNC
- HGNC:37197 HGNC
- Ensembl
- ENSG00000241369 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Ranking
ClinVar | |
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0 |
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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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 |
---|---|---|---|---|---|
ENST00000655584.1 | hg38 | chr3 | 163,199,575 | 163,303,283 | 103,709 |
ENST00000658280.1 | hg38 | chr3 | 163,109,697 | 163,304,719 | 195,023 |
ENST00000670655.1 | hg38 | chr3 | 163,109,757 | 163,303,314 | 193,558 |
ENST00000667319.1 | hg38 | chr3 | 163,182,735 | 163,303,339 | 120,605 |
ENST00000662016.1 | hg38 | chr3 | 163,199,578 | 163,304,685 | 105,108 |
ENST00000654755.1 | hg38 | chr3 | 163,215,635 | 163,304,773 | 89,139 |
ENST00000489012.5 | hg38 | chr3 | 163,199,623 | 163,361,563 | 161,941 |
ENST00000657261.1 | hg38 | chr3 | 163,127,915 | 163,303,324 | 175,410 |
ENST00000660789.1 | hg38 | chr3 | 163,109,152 | 163,303,309 | 194,158 |
ENST00000666234.1 | hg38 | chr3 | 163,109,811 | 163,303,323 | 193,513 |
ENST00000660789.1 | hg19 | chr3 | 162,826,940 | 163,021,097 | 194,158 |
ENST00000657261.1 | hg19 | chr3 | 162,845,703 | 163,021,112 | 175,410 |
ENST00000658280.1 | hg19 | chr3 | 162,827,485 | 163,022,507 | 195,023 |
ENST00000662016.1 | hg19 | chr3 | 162,917,366 | 163,022,473 | 105,108 |
ENST00000654755.1 | hg19 | chr3 | 162,933,423 | 163,022,561 | 89,139 |
ENST00000489012.5 | hg19 | chr3 | 162,917,411 | 163,079,351 | 161,941 |
ENST00000666234.1 | hg19 | chr3 | 162,827,599 | 163,021,111 | 193,513 |
ENST00000655584.1 | hg19 | chr3 | 162,917,363 | 163,021,071 | 103,709 |
ENST00000667319.1 | hg19 | chr3 | 162,900,523 | 163,021,127 | 120,605 |
ENST00000670655.1 | hg19 | chr3 | 162,827,545 | 163,021,102 | 193,558 |
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