LINC01498 long intergenic non-protein coding RNA 1498
Information
- Symbol
- LINC01498
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1498
- Entrez Gene ID
- 102723562
- Genome
- hg19
- Position
- chr12:108,827,907-108,886,362
- Genome
- hg38
- Position
- chr12:108,434,130-108,492,585
- HGNC
- HGNC:51164 HGNC
- Ensembl
- ENSG00000247213 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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
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 |
---|---|---|---|---|---|
ENST00000502160.6 | hg38 | chr12 | 108,434,130 | 108,492,585 | 58,456 |
ENST00000670674.1 | hg38 | chr12 | 108,491,576 | 108,515,023 | 23,448 |
ENST00000502160.6 | hg19 | chr12 | 108,827,907 | 108,886,362 | 58,456 |
ENST00000670674.1 | hg19 | chr12 | 108,885,353 | 108,908,800 | 23,448 |
Genome browser