LINC00507 long intergenic non-protein coding RNA 507
Information
- Symbol
- LINC00507
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 507
- Entrez Gene ID
- 100862680
- Genome
- hg19
- Position
- chr12:128,399,947-128,436,097
- Genome
- hg38
- Position
- chr12:127,915,402-127,951,552
- HGNC
- HGNC:43558 HGNC
- Ensembl
- ENSG00000256193 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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
[No Data.]
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| 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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| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000657939.1 | hg38 | chr12 | 127,915,407 | 127,951,430 | 36,024 |
| ENST00000667075.1 | hg38 | chr12 | 127,915,402 | 127,951,552 | 36,151 |
| ENST00000662793.1 | hg38 | chr12 | 127,915,218 | 127,951,357 | 36,140 |
| ENST00000670551.1 | hg38 | chr12 | 127,915,382 | 127,950,370 | 34,989 |
| ENST00000657939.1 | hg19 | chr12 | 128,399,952 | 128,435,975 | 36,024 |
| ENST00000662793.1 | hg19 | chr12 | 128,399,763 | 128,435,902 | 36,140 |
| ENST00000667075.1 | hg19 | chr12 | 128,399,947 | 128,436,097 | 36,151 |
| ENST00000670551.1 | hg19 | chr12 | 128,399,927 | 128,434,915 | 34,989 |
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