LINC01206 long intergenic non-protein coding RNA 1206
Information
- Symbol
- LINC01206
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1206
- Entrez Gene ID
- 100996490
- Genome
- hg19
- Position
- chr3:181,670,131-181,728,466
- Genome
- hg38
- Position
- chr3:181,952,343-182,010,678
- HGNC
- HGNC:49637 HGNC
- Ensembl
- ENSG00000242512 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
not provided | 1 | 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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Category | : |
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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 |
---|---|---|---|---|---|
ENST00000662045.1 | hg38 | chr3 | 181,952,373 | 182,004,063 | 51,691 |
ENST00000655047.1 | hg38 | chr3 | 181,952,394 | 182,003,122 | 50,729 |
ENST00000658146.1 | hg38 | chr3 | 181,952,360 | 182,003,140 | 50,781 |
ENST00000668631.1 | hg38 | chr3 | 181,952,397 | 182,003,122 | 50,726 |
ENST00000482787.7 | hg38 | chr3 | 181,952,343 | 182,010,678 | 58,336 |
ENST00000654624.1 | hg38 | chr3 | 181,952,383 | 182,001,674 | 49,292 |
ENST00000609168.2 | hg38 | chr3 | 181,971,216 | 181,976,459 | 5,244 |
ENST00000653068.1 | hg38 | chr3 | 181,952,376 | 182,001,858 | 49,483 |
ENST00000656291.1 | hg38 | chr3 | 181,952,370 | 182,003,122 | 50,753 |
ENST00000654438.1 | hg38 | chr3 | 181,970,445 | 182,004,053 | 33,609 |
ENST00000662045.1 | hg19 | chr3 | 181,670,161 | 181,721,851 | 51,691 |
ENST00000482787.7 | hg19 | chr3 | 181,670,131 | 181,728,466 | 58,336 |
ENST00000609168.2 | hg19 | chr3 | 181,689,004 | 181,694,247 | 5,244 |
ENST00000653068.1 | hg19 | chr3 | 181,670,164 | 181,719,646 | 49,483 |
ENST00000656291.1 | hg19 | chr3 | 181,670,158 | 181,720,910 | 50,753 |
ENST00000654438.1 | hg19 | chr3 | 181,688,233 | 181,721,841 | 33,609 |
ENST00000658146.1 | hg19 | chr3 | 181,670,148 | 181,720,928 | 50,781 |
ENST00000654624.1 | hg19 | chr3 | 181,670,171 | 181,719,462 | 49,292 |
ENST00000655047.1 | hg19 | chr3 | 181,670,182 | 181,720,910 | 50,729 |
ENST00000668631.1 | hg19 | chr3 | 181,670,185 | 181,720,910 | 50,726 |
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