LINC00354 long intergenic non-protein coding RNA 354
Information
- Symbol
- LINC00354
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 354
- Entrez Gene ID
- 101928616
- Genome
- hg19
- Position
- chr13:112,547,582-112,555,578
- Genome
- hg38
- Position
- chr13:111,893,268-111,901,264
- HGNC
- HGNC:42672 HGNC
- Ensembl
- ENSG00000226903 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 |
---|---|---|---|---|---|
ENST00000661311.1 | hg38 | chr13 | 111,893,745 | 111,901,081 | 7,337 |
ENST00000670855.1 | hg38 | chr13 | 111,893,375 | 111,901,176 | 7,802 |
ENST00000662993.1 | hg38 | chr13 | 111,893,268 | 111,901,264 | 7,997 |
ENST00000662993.1 | hg19 | chr13 | 112,547,582 | 112,555,578 | 7,997 |
ENST00000670855.1 | hg19 | chr13 | 112,547,689 | 112,555,490 | 7,802 |
ENST00000661311.1 | hg19 | chr13 | 112,548,059 | 112,555,395 | 7,337 |
Genome browser